GapMind for catabolism of small carbon sources

 

Aligments for a candidate for xylF in Marinobacter adhaerens HP15

Align 2-hydroxymuconate-6-semialdehyde hydrolase (EC 3.7.1.9) (characterized)
to candidate GFF1134 HP15_1112 2-hydroxymuconic semialdehyde hydrolase

Query= BRENDA::G3KFX4
         (282 letters)



>lcl|FitnessBrowser__Marino:GFF1134 HP15_1112 2-hydroxymuconic
           semialdehyde hydrolase
          Length = 286

 Score =  455 bits (1171), Expect = e-133
 Identities = 216/279 (77%), Positives = 249/279 (89%), Gaps = 1/279 (0%)

Query: 1   MNAPQQSPEIGREILAAGYRTNLHDQGEG-FPVLLIHGSGPGVTAWANWRLVMPQLAQNR 59
           M  P++SPEIGREI AAGYRTN+HD GEG  PV++IHGSGPGVTAWANWRLV+P+LA+NR
Sbjct: 1   MTVPEKSPEIGREITAAGYRTNVHDHGEGGVPVMMIHGSGPGVTAWANWRLVIPELAKNR 60

Query: 60  RVIAPDMLGFGYSDRPADGRYHQQRWVEHAIGVLDALGIQQADIVGNSFGGGLALALAIR 119
           RV+APDMLGFGYS+RP D  Y+++RWV+HAIGV+D LG++Q D+VGNSFGGGLALALAI 
Sbjct: 61  RVVAPDMLGFGYSERPEDQIYNRERWVKHAIGVMDELGLEQVDLVGNSFGGGLALALAIE 120

Query: 120 HPERVRRLVLMGSVGVSFPITPGLDAVWGYEPSFASMRRLMDVFAYDRSLVTNELAELRY 179
           HP+R+RRLVLMGS GV FPIT GLD VWGYEPS  +MRRLMDVFA+++ L+T+ELAE+RY
Sbjct: 121 HPKRIRRLVLMGSAGVRFPITEGLDEVWGYEPSLDNMRRLMDVFAFNKGLLTDELAEMRY 180

Query: 180 QASIRPGFQESFAQMFPAPRQRWVDGLASDEADIRALPHETLVIHGREDQVIPLAASLTL 239
           +ASIRPGFQESFA MFPAPRQRWVD LAS+E DIRAL HETL+IHGRED+VIPL ASL L
Sbjct: 181 EASIRPGFQESFAAMFPAPRQRWVDNLASNEDDIRALTHETLIIHGREDEVIPLEASLRL 240

Query: 240 AEWIARAQLHVFGHCGHWTQIEHAERFARLVENFLAEAD 278
           AE I RAQLHVFG CGHWTQIEHA+RFARLV +FL EAD
Sbjct: 241 AELIDRAQLHVFGRCGHWTQIEHADRFARLVNDFLTEAD 279


Lambda     K      H
   0.323    0.138    0.432 

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: 406
Number of extensions: 18
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: 282
Length of database: 286
Length adjustment: 26
Effective length of query: 256
Effective length of database: 260
Effective search space:    66560
Effective search space used:    66560
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 47 (22.7 bits)

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

Links

Downloads

Related tools

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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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