diff --git a/docs/ensembl_das/Homo_sapiens.ini b/docs/ensembl_das/Homo_sapiens.ini
index 2b17b99e82168391cad89485464e49ba2e589172..b80c33496d7eb635aafac363daa129570d65b2db 100644
--- a/docs/ensembl_das/Homo_sapiens.ini
+++ b/docs/ensembl_das/Homo_sapiens.ini
@@ -22,25 +22,17 @@
 # Assembly info
 ENSEMBL_PREFIX          = ENS           ; EnsEMBL gene id prefix
 ENSEMBL_GOLDEN_PATH     = NCBI34       ; Indentifier for the golden path type
-ASSEMBLY_STATUS         = FULL
 ENSEMBL_CHROMOSOMES     = [ 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y ]
 
 # Search config
 ; list of features that are indexed ready for searching
 ENSEMBL_SEARCH_IDXS     = [ Disease Domain EST External Family Gene MRNA Marker Peptide Protein SNP SangerProject Sequence Unigene ]
 
-# Das - default DAS mapmaster for "uploadable DAS"
-ENSEMBL_DAS_MAPMASTER_DSN = ensembl1834
-
-# Biggest unit of mapping
-ENSEMBL_BUM = Chromosome
 
 # Display info
 SPECIES_COMMON_NAME     = Human
 SPECIES_BIO_NAME        = Homo sapiens
 SPECIES_CODE            = hs
-GENERATE_HOME_PAGE      = yes
-CYTOVIEW_ENABLED        = 1
 
 ENSEMBL_PREDICTION_TEXT_CORE    = Genes were annotated by the Ensembl automatic analysis pipeline using either a GeneWise model from a human/vertebrate protein, a set of aligned human cDNAs followed by GenomeWise for ORF prediction or from Genscan exons supported by protein, cDNA and EST evidence. GeneWise models are further combined with available aligned cDNAs to annotate UTRs.
 ENSEMBL_PREDICTION_TEXT_PSEUDOGENE    = Potential processed pseudogenes are detected from genewise predictions that have a single-exon with frameshifts, have their evidence spliced elsewhere in the genome and have no match in the syntenic genomic region in mouse.
@@ -56,13 +48,7 @@ ENSEMBL_PREDICTION_TEXT_VEGA	= Finished genomic sequence is analysed on a clone
 [databases]
 
 ENSEMBL_DB              = homo_sapiens_core_19_34b
-ENSEMBL_DISEASE         = homo_sapiens_disease_19_34b
-ENSEMBL_EST		= homo_sapiens_est_19_34b
-ENSEMBL_ESTGENE		= homo_sapiens_estgene_19_34b
-ENSEMBL_HAPLOTYPE       = homo_sapiens_haplotype_19_34b
-ENSEMBL_LITE            = homo_sapiens_lite_19_34b
 ENSEMBL_VEGA            = homo_sapiens_vega_19_34b
-ENSEMBL_SNP             = homo_sapiens_snp_19_34b
 
 # The following are extra configuration parameters for the databases
 # You can overide the default settings for specific databases. Just add a
@@ -79,7 +65,7 @@ ENSEMBL_SNP             = homo_sapiens_snp_19_34b
 # Help Database Config
 ####################
 
-[ENSEMBL_HELP] 
+[ENSEMBL_WEBSITE] 
 # Accept defaults