GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Luteimonas huabeiensis HB2

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_024890485.1 Z164_RS0109600 acyl-CoA dehydrogenase

Query= metacyc::G1G01-166-MONOMER
         (393 letters)



>NCBI__GCF_000559025.1:WP_024890485.1
          Length = 382

 Score =  213 bits (541), Expect = 1e-59
 Identities = 134/378 (35%), Positives = 206/378 (54%), Gaps = 8/378 (2%)

Query: 20  TEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAI-FREMGEVGLLGATIPEQYGGSGL 78
           +EE+ M++D A + AQ+++AP   EAF      P    R +GE GL+G  +P +YGG+G+
Sbjct: 6   SEEQLMIQDVARRIAQERIAPSA-EAFDRSGEFPLENIRLLGENGLMGIEVPTEYGGAGM 64

Query: 79  NYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASGEWIGCFG 138
           + V Y L   E+   D+ + ++MSV +SL    I   GTEAQKQ Y+  +A G  IG F 
Sbjct: 65  DPVAYVLAMVEIAAADAAHSTIMSVNNSLFCNGILTHGTEAQKQTYVRAIAEGREIGAFA 124

Query: 139 LTEPNHGSDPGSMITRA-RKVDGGYRLTGSKMWITNSPIADVFVVWAKDD----AGDIRG 193
           LTEP  GSD  SM  RA  + DG + + G K WIT+ P+A   V++A  D    A  I  
Sbjct: 125 LTEPQSGSDATSMRCRAVAQADGSFVVNGKKSWITSGPVARYIVLFATTDPAQGARGITA 184

Query: 194 FVLEKGWQGLSAPAIHGKVGLRASITGEI-VMDNVFVPEENIFPDVRGLKGPFTCLNSAR 252
           F+++   +G        K+G+RAS T EI   D V   +E +    +G K   + L++ R
Sbjct: 185 FLVDTQREGFHRGKTEPKLGIRASATCEIEFQDYVVRADEVLGQPGQGFKIAMSVLDAGR 244

Query: 253 YGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCLRLG 312
            GI+  A+G A A +     Y  +R+ FG+P+ A Q+ Q K+ADM+ ++  +L   LR  
Sbjct: 245 IGIASQAIGIARAAYEATIAYVKERKAFGQPIGAFQMTQAKIADMKCKLDASLLLTLRAA 304

Query: 313 RMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLEVVNTYE 372
            +K +G       S+ K  +   A+ IA  A  + GG G S E  V R+  + ++   YE
Sbjct: 305 WLKRQGQRFTTEASVAKLTASEAAMWIAHQAVQIHGGMGYSKEMPVERYFRDAKITEIYE 364

Query: 373 GTHDVHALILGRAQTGIQ 390
           GT ++  L++ R +TG++
Sbjct: 365 GTSEIQRLVIARNETGLR 382


Lambda     K      H
   0.320    0.137    0.413 

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: 355
Number of extensions: 21
Number of successful extensions: 5
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: 393
Length of database: 382
Length adjustment: 30
Effective length of query: 363
Effective length of database: 352
Effective search space:   127776
Effective search space used:   127776
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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