Alignments for a candidate for gcvP in Thermocrinis albus DSM 14484

GapMind for catabolism of small carbon sources

Alignments for a candidate for gcvP in Thermocrinis albus DSM 14484

Align Probable glycine dehydrogenase (decarboxylating) subunit 2; EC 1.4.4.2; Glycine cleavage system P-protein subunit 2; Glycine decarboxylase subunit 2; Glycine dehydrogenase (aminomethyl-transferring) subunit 2 (uncharacterized)
to candidate WP_012992260.1 THAL_RS06225 aminomethyl-transferring glycine dehydrogenase subunit GcvPB

Query= curated2:O67740
         (482 letters)



>NCBI__GCF_000025605.1:WP_012992260.1
          Length = 477

 Score =  708 bits (1827), Expect = 0.0
 Identities = 347/476 (72%), Positives = 402/476 (84%), Gaps = 1/476 (0%)

Query: 1   MELIFEKSKKGRKGYKLPELDVEEVNIKEYLPEEYLREELDFPEVSELDVVRHYTNLSHL 60
           MELIFEKS  GR+GY LP LDV EV++K YL E Y RE+L  PEVS+LDVVRHYT LS L
Sbjct: 1   MELIFEKSSPGRRGYHLPPLDVPEVDLKGYLGEFY-REDLPLPEVSQLDVVRHYTKLSQL 59

Query: 61  NYAVDTTMVPLGSCTMKYNPRINEELVNKKEFLNVHPLTPEEYIQPLLKLVYELKELLKE 120
           NYA+DTTMVPLGSCTMKYNPRINEELV  + F +VHP+ PEE +Q  L+L+Y+LKELLKE
Sbjct: 60  NYAIDTTMVPLGSCTMKYNPRINEELVQMEGFRDVHPMAPEETVQGTLQLLYQLKELLKE 119

Query: 121 LGGFAEVSLQPAAGAHGELLGLLLIHAYHQDRGNKEKKVVLIPDSAHGTNPASAAICGFD 180
           LGGFA+VSLQPAAGA GE LGLL+I AYH+DRGN  K+ VL+PD+AHGTNPASAAICGF+
Sbjct: 120 LGGFADVSLQPAAGAQGEFLGLLMILAYHRDRGNHHKRKVLVPDTAHGTNPASAAICGFE 179

Query: 181 IKVVKSDKKGELDFEDFIKKLDERVAALMITNPNTLGIFERKIKEIAEELHKRDALLYMD 240
           +  VKS+K GELD++DF  KL + VA LM+TNPNTLGIFER+IK+IA+ LH  DALLYMD
Sbjct: 180 VVTVKSNKDGELDWDDFKSKLRDDVACLMLTNPNTLGIFERRIKQIADALHSMDALLYMD 239

Query: 241 GANFNALVGRFKPGEWGVDVMHFNLHKTFSTPHGGGGPGAGPVGVSERLKPYLPVPQIEY 300
           GANFNALVG  KPG+WGVDVMHFNLHKTFSTPHGGGGPG G VGVSE+L+PYLPVPQ+E+
Sbjct: 240 GANFNALVGVAKPGDWGVDVMHFNLHKTFSTPHGGGGPGGGAVGVSEKLRPYLPVPQVEF 299

Query: 301 DGKKYYLNWNIEKSVGKILAFHGHFLVWLKALAYILTYGKDIKKVSEYAVLNARYLKHLL 360
           DG++YYLNWNI KSVGK+LAF+GH  V L+ALAYIL+YG +I  V++YAVLNARYL HL+
Sbjct: 300 DGERYYLNWNIPKSVGKVLAFYGHTAVSLRALAYILSYGNNIDLVAKYAVLNARYLHHLI 359

Query: 361 KGVFKDPYPESPCMHEFVLSATNLTKYGVRASDVAKRILDYGFYAPTMYFPLIVREALMI 420
           K +F DPYP  P MHE VLSA NL KYGV A DVAK +LD GFYAPT+YFPL V+EALMI
Sbjct: 360 KDLFVDPYPHVPRMHEMVLSAANLNKYGVGAMDVAKALLDMGFYAPTVYFPLTVKEALMI 419

Query: 421 EPTETENPDTLKKFALILRKIVKEAKEKPEILKKAPHRTPVRRIKEAEANRNLILK 476
           EPTETE+P TL+ FA  LR IV+ AKE P+ LK+AP RTPVRRIKEAEANR  +L+
Sbjct: 420 EPTETESPQTLEAFAEALRSIVRTAKENPDALKEAPKRTPVRRIKEAEANRRPVLR 475


Lambda     K      H
   0.318    0.139    0.407 

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: 718
Number of extensions: 26
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: 482
Length of database: 477
Length adjustment: 34
Effective length of query: 448
Effective length of database: 443
Effective search space:   198464
Effective search space used:   198464
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: 41 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources