GapMind for catabolism of small carbon sources

 

Alignments for a candidate for hmgA in Shewanella loihica PV-4

Align Homogentisate 1,2-dioxygenase (EC 1.13.11.5) (characterized)
to candidate 5209701 Shew_2154 homogentisate 1,2-dioxygenase (RefSeq)

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



>FitnessBrowser__PV4:5209701
          Length = 386

 Score =  729 bits (1882), Expect = 0.0
 Identities = 330/386 (85%), Positives = 366/386 (94%)

Query: 1   MPFYVKQGQVPHKRHIAFEKENGELYREELFSTHGFSNIYSNKYHHNMPTKALEVAPYRL 60
           MPFYV+QG++PHKRHI F+KENGELYREELFSTHGFSNIYSNKYHHNMPTKALEV+P+ +
Sbjct: 1   MPFYVRQGEIPHKRHITFKKENGELYREELFSTHGFSNIYSNKYHHNMPTKALEVSPFEV 60

Query: 61  GHGAHWEDSLVQNYKLDSRSADREGNFFSARNKIFYNNDVAIYTAKVTQDTAEFYRNAYA 120
            HG  W+D+L+QNYKLD++ ADREGNF+SARNKIF+NNDVA+Y+AKVT+ T EFYRNAYA
Sbjct: 61  NHGQTWQDTLIQNYKLDAKLADREGNFYSARNKIFFNNDVAMYSAKVTEATEEFYRNAYA 120

Query: 121 DEVVFVHEGEGTLYSEYGTLEIKKWDYLVIPRGTTHQLKFNNYSNVRLFVIEAFSMVEVP 180
           DEV+FVHEG+G LYSEYG L++KKWDYLVIPRGTT+QLKF++YS VRLFVIEAFSMVEVP
Sbjct: 121 DEVIFVHEGQGKLYSEYGVLDVKKWDYLVIPRGTTYQLKFDDYSQVRLFVIEAFSMVEVP 180

Query: 181 KHCRNEYGQLLESAPYCERDLRTPILQAAVVERGAFPLVCKFGDKYQLTTLEWHPFDLVG 240
           KH RNEYGQLLESAPYCERD+R P LQ AVVE+GAFPLVCKFGDKYQLT LEWHPFDLVG
Sbjct: 181 KHFRNEYGQLLESAPYCERDIRVPSLQEAVVEKGAFPLVCKFGDKYQLTQLEWHPFDLVG 240

Query: 241 WDGCVYPWAFNITEYAPKVGKIHLPPSDHLVFTAHNFVVCNFVPRPYDFHERAIPAPYYH 300
           WDGCVYPWAFNI +YAPKVG+IHLPPSDHLVFTAHNFV+CNFVPRPYDFH ++IPAPYYH
Sbjct: 241 WDGCVYPWAFNIQDYAPKVGQIHLPPSDHLVFTAHNFVICNFVPRPYDFHPQSIPAPYYH 300

Query: 301 NNIDSDEVLYYVDGDFMSRTGIEAGYITLHQKGVAHGPQPGRTEASIGKKETYEYAVMVD 360
           NNIDSDEVLYYVDGDFMSRTGIEAGY+TLHQKGV HGPQPGRTEAS+GKKETYEYAVMVD
Sbjct: 301 NNIDSDEVLYYVDGDFMSRTGIEAGYMTLHQKGVPHGPQPGRTEASVGKKETYEYAVMVD 360

Query: 361 TFAPLKLTEHVQHCMSKDYNRSWLEN 386
           TFAPL+LT+HVQ CMSKDYNRSWLE+
Sbjct: 361 TFAPLQLTQHVQGCMSKDYNRSWLED 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: 749
Number of extensions: 26
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.

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:

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