GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Maridesulfovibrio bastinii DSM 16055

Align Predicted serC by GapMind curators (no experimental data)
to candidate WP_027177954.1 G496_RS0102925 aminotransferase class V-fold PLP-dependent enzyme

Query= predicted:A0A1T4W7T3
         (378 letters)



>NCBI__GCF_000429985.1:WP_027177954.1
          Length = 379

 Score =  451 bits (1159), Expect = e-131
 Identities = 227/375 (60%), Positives = 284/375 (75%)

Query: 1   MSTQDFAALKLFITGPTLLRPEVRQAGTLPEFGHRDSENLKRLEPAMHWLAELADAGDQY 60
           M   DFA L+LFITGP LLR EVR+AG LPEFGHRDSEN+KR  P M  L +L+ A + Y
Sbjct: 1   MIGSDFAELQLFITGPILLRKEVREAGLLPEFGHRDSENVKRFGPIMENLRKLSGAPEDY 60

Query: 61  TPVLFLGSGSTGLEAAVRSLVAEDETVLNVSVGAFGDLFHSMAVANGKRAVQLKFDMGRA 120
             ++F GSG+  LEA+VRSLVA D+TVLNVSVGAFGDL+H +AV NGK AVQLKFD GRA
Sbjct: 61  DIIIFNGSGTNVLEASVRSLVASDDTVLNVSVGAFGDLYHKLAVTNGKNAVQLKFDYGRA 120

Query: 121 IDLDELDRALTEHRPGVVTFTHNETSTGVINDIHAVTELVRRRGALSVVDGVSIFGGTEL 180
           IDLD+L++AL E+ P VVTFT NETSTGV N++  V  L+ + GA S+VD VSIFGG   
Sbjct: 121 IDLDKLEQALEEYSPDVVTFTQNETSTGVFNNVPEVCALIHKYGAKSLVDAVSIFGGAPS 180

Query: 181 GLKDSGIAMYCSATQKSLALPAGFGIGLIHAEAAEKAARVTNKGHGSDILKHLDKARKFQ 240
            + ++   MY ++TQKSL LPAGFGI  +  E  EKA +V N+G+ +DIL  ++KAR  Q
Sbjct: 181 CIAEAKPMMYSTSTQKSLGLPAGFGIAFVSPEGFEKAEKVENRGYTTDILAQVEKARNLQ 240

Query: 241 TLSTPNTTLANQLYVQLRYIMEEEGMARRFARHRAMREMVARWVDGLEGFRLFAQEGFRS 300
           TL+TPN TL NQ+ VQL YI+ +E + +RFARH  MREM   WV+ ++G+ LFAQEG+RS
Sbjct: 241 TLTTPNGTLVNQMCVQLDYIVNDETIEKRFARHEEMREMAHEWVEQMDGYSLFAQEGYRS 300

Query: 301 PALTTVQVPDGVSVQQLKQVKETMRARGYLFDPGYGKLNTELEASGRAPIFRVGHMGDIT 360
           P+++ VQ   G++V++LKQVKE MR  GYLFDPGYGK+N ELEASGR PIFR+GHM DI+
Sbjct: 301 PSVSAVQTAPGMTVEKLKQVKEAMRGHGYLFDPGYGKINKELEASGRQPIFRIGHMADIS 360

Query: 361 PAMLEEYLGELGEVL 375
           P ML++YL  L  VL
Sbjct: 361 PEMLKKYLEILSGVL 375


Lambda     K      H
   0.319    0.135    0.387 

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: 420
Number of extensions: 17
Number of successful extensions: 1
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: 378
Length of database: 379
Length adjustment: 30
Effective length of query: 348
Effective length of database: 349
Effective search space:   121452
Effective search space used:   121452
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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