GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Desulfuromonas acetexigens

Align cystathionine gamma-lyase (EC 4.4.1.1); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized)
to candidate WP_092055964.1 BQ4888_RS07650 PLP-dependent transferase

Query= BRENDA::A2RM21
         (380 letters)



>NCBI__GCF_900111775.1:WP_092055964.1
          Length = 380

 Score =  361 bits (926), Expect = e-104
 Identities = 180/372 (48%), Positives = 262/372 (70%), Gaps = 1/372 (0%)

Query: 6   TKVIHGGISTDKTTGAVSVPIYQTSTYKQNGLGQPKEYEYSRSGNPTRHALEELIADLEG 65
           T ++H GI  D  TGA ++PIYQ STY   G GQP EY+Y+RSGNP+R  +E+ IA LEG
Sbjct: 10  TLLVHQGIDRDPATGASAIPIYQASTYHHVG-GQPGEYDYARSGNPSRRQVEDAIALLEG 68

Query: 66  GVQGFAFSSGLAGIHAVLSLFSAGDHIILADDVYGGTFRLMDKVLTKTGIIYDLVDLSNL 125
           GV+GFA+++G+A I + L+L  +GDH+I  +D+YGG++R +  VL + GI    VD+++L
Sbjct: 69  GVRGFAYATGMAAIGSALALLKSGDHLIAPNDLYGGSWRYLSTVLPEQGITTSFVDITDL 128

Query: 126 DDLKAAFKEETKAIYFETPSNPLLKVLDIKEISAIAKAHDALTLVDNTFATPYLQQPIAL 185
           + ++AA    TKAI+ ETPSNPL  + DI+ ++A+A+    LTL+DNTF TP LQ+P+ L
Sbjct: 129 NRIEAAITPATKAIFLETPSNPLFNITDIRAVTALARQRGLLTLLDNTFMTPLLQRPLEL 188

Query: 186 GADIVLHSATKYLGGHSDVVAGLVTTNSKELASEIGFLQNSIGAVLGPQDSWLVQRGIKT 245
           G D+V+HSATK+LGGHSD++AGLVTT   +LA  + + QN+ GAVL P DS+L+ RGIKT
Sbjct: 189 GVDVVIHSATKFLGGHSDLMAGLVTTADPQLAKRLKYFQNAFGAVLAPFDSFLLARGIKT 248

Query: 246 LALRMEAHSANAQKIAEFLETSKAVSKVYYPGLNSHPGHEIAKKQMSAFGGMISFELTDE 305
           L LR+EA   +AQ +AE L+   AV++V++PGL    G E+   Q S  G ++SFEL ++
Sbjct: 249 LKLRLEAAQRSAQDLAERLQDHPAVARVWFPGLVDFAGRELHFSQASGAGAVLSFELKEQ 308

Query: 306 NAVKDFVENLSYFTLAESLGGVESLIEVPAVMTHASIPKELREEIGIKDGLIRLSVGVEA 365
             V   ++ +    +A SLGGVE+++     M+HA+IP E +  +GI++ L+R+SVG+E 
Sbjct: 309 ARVAPLLQQIKLPIIAPSLGGVETILTHCWSMSHAAIPAETKLRLGIRETLLRISVGIED 368

Query: 366 IEDLLTDIKEAL 377
           +EDL  D+  AL
Sbjct: 369 VEDLWEDLAAAL 380


Lambda     K      H
   0.315    0.133    0.366 

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: 414
Number of extensions: 11
Number of successful extensions: 2
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: 380
Length of database: 380
Length adjustment: 30
Effective length of query: 350
Effective length of database: 350
Effective search space:   122500
Effective search space used:   122500
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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