GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Desulfovibrio vulgaris Miyazaki F

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate 8501944 DvMF_2658 cysteine synthase (RefSeq)

Query= metacyc::MONOMER-20568
         (299 letters)



>FitnessBrowser__Miya:8501944
          Length = 310

 Score =  229 bits (585), Expect = 5e-65
 Identities = 124/301 (41%), Positives = 176/301 (58%), Gaps = 10/301 (3%)

Query: 5   NILETIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKLHPGS 64
           ++ E +G TPLVR+N ++     ++ AKLE  NP  SVKDRIAL MI+ A   G+L PG 
Sbjct: 6   DMTELVGRTPLVRLNRVSEGCAAEVVAKLEFNNPCASVKDRIALAMIDGAMERGELAPGG 65

Query: 65  TIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKKLGTDGA 124
            ++E TSGNTG+GLA +  V+G  +++ M E +S ER+ +++ FGA ++LT    G  GA
Sbjct: 66  LLVEPTSGNTGVGLAFVAAVRGLTLVLTMPESMSNERKALLRGFGARLVLTPASKGMRGA 125

Query: 125 IRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVGTSGTLM 184
           I +   +V E PG      QF N  N + H KTTAEEIWA T G V  FVA VGT GT+ 
Sbjct: 126 IEEAERIVAETPGAVM-LGQFVNPDNPLVHRKTTAEEIWADTDGKVDAFVAGVGTGGTVT 184

Query: 185 GVGKNLREKNPEIKIIEAQPTKGHYIQG-------LKSMEEAIVPAIYQADKIDEHILIE 237
           G G+ LRE NP+IK+   +P +   + G       ++ +    VP +      DE I + 
Sbjct: 185 GTGRRLRELNPDIKVFAVEPDESPVLSGGAPGPHPIQGIGAGFVPPVLDTKVYDEIIRVP 244

Query: 238 SEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDSG--VIVVLFADRGEKYLSTKL 295
            ++A   AR ++ +EGI  G+SSGA   AA  +A + +     +V +  D GE+YLST L
Sbjct: 245 GKDALVTARRLLREEGILCGVSSGANAFAAMAVARRPEMAGKRVVFVVCDTGERYLSTPL 304

Query: 296 F 296
           F
Sbjct: 305 F 305


Lambda     K      H
   0.315    0.133    0.367 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 294
Number of extensions: 18
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 299
Length of database: 310
Length adjustment: 27
Effective length of query: 272
Effective length of database: 283
Effective search space:    76976
Effective search space used:    76976
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory