GapMind for catabolism of small carbon sources

 

Alignments for a candidate for hmgA in Shewanella amazonensis SB2B

Align Homogentisate 1,2-dioxygenase (EC 1.13.11.5) (characterized)
to candidate 6937405 Sama_1569 homogentisate 1,2-dioxygenase (RefSeq)

Query= reanno::MR1:201124
         (386 letters)



>FitnessBrowser__SB2B:6937405
          Length = 386

 Score =  724 bits (1870), Expect = 0.0
 Identities = 339/386 (87%), Positives = 360/386 (93%)

Query: 1   MPFYVKQGQVPHKRHIAFEKENGELYREELFSTHGFSNIYSNKYHHNMPTKALEVAPYRL 60
           MPFYVKQGQ+PHKRHIAF KENGELYREELFSTHGFSNIYSNKYHHNMPTKALEVAP  L
Sbjct: 1   MPFYVKQGQIPHKRHIAFAKENGELYREELFSTHGFSNIYSNKYHHNMPTKALEVAPMSL 60

Query: 61  GHGAHWEDSLVQNYKLDSRSADREGNFFSARNKIFYNNDVAIYTAKVTQDTAEFYRNAYA 120
            HG  W DSLVQNYKLDSR AD EGNFFSARNKIF+N DVA+YTAKVT DT EFYRNAYA
Sbjct: 61  THGDTWVDSLVQNYKLDSRLADGEGNFFSARNKIFFNADVALYTAKVTADTDEFYRNAYA 120

Query: 121 DEVVFVHEGEGTLYSEYGTLEIKKWDYLVIPRGTTHQLKFNNYSNVRLFVIEAFSMVEVP 180
           DEVVFVHEG+G L SEYG LE+KKWDYLVIPRGTT+QLKFN+YSNVRLFVIE+F+MVE+P
Sbjct: 121 DEVVFVHEGDGVLLSEYGELEVKKWDYLVIPRGTTYQLKFNDYSNVRLFVIESFTMVEIP 180

Query: 181 KHCRNEYGQLLESAPYCERDLRTPILQAAVVERGAFPLVCKFGDKYQLTTLEWHPFDLVG 240
           KH RNEYGQLLESAPYCERD+R P L+ AVVERG FPLVCKFGDKYQLT LEWHPFDLVG
Sbjct: 181 KHFRNEYGQLLESAPYCERDIRVPELKDAVVERGNFPLVCKFGDKYQLTQLEWHPFDLVG 240

Query: 241 WDGCVYPWAFNITEYAPKVGKIHLPPSDHLVFTAHNFVVCNFVPRPYDFHERAIPAPYYH 300
           WDG VYPWAFNITEYAPKVGKIHLPPSDHL+F A NFV+CNFVPRPYDFH +AIPAPYYH
Sbjct: 241 WDGFVYPWAFNITEYAPKVGKIHLPPSDHLLFVARNFVICNFVPRPYDFHPQAIPAPYYH 300

Query: 301 NNIDSDEVLYYVDGDFMSRTGIEAGYITLHQKGVAHGPQPGRTEASIGKKETYEYAVMVD 360
           NNIDSDEVLYYVDGDFMSRTGIEAGYITLHQKGVAHGPQPGRTEASIGKK+TYEYAVMVD
Sbjct: 301 NNIDSDEVLYYVDGDFMSRTGIEAGYITLHQKGVAHGPQPGRTEASIGKKDTYEYAVMVD 360

Query: 361 TFAPLKLTEHVQHCMSKDYNRSWLEN 386
           TFAPL+LTEHV++CM+ DYNRSWLE+
Sbjct: 361 TFAPLQLTEHVKNCMAPDYNRSWLED 386


Lambda     K      H
   0.321    0.137    0.435 

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: 741
Number of extensions: 23
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: 386
Length of database: 386
Length adjustment: 30
Effective length of query: 356
Effective length of database: 356
Effective search space:   126736
Effective search space used:   126736
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 17 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