GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Stutzerimonas stutzeri A1501

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate WP_011913323.1 PST_RS11065 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:Q6MNM2
         (347 letters)



>NCBI__GCF_000013785.1:WP_011913323.1
          Length = 371

 Score =  305 bits (780), Expect = 2e-87
 Identities = 165/363 (45%), Positives = 228/363 (62%), Gaps = 31/363 (8%)

Query: 1   MAKIQFSNIKKSFGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTI 60
           MA ++  N+KK F   +++KGIDLDI   EF+V VGPSGCGKSTLLR +AGLE   SG I
Sbjct: 1   MADLKIHNLKKGFDGNEIIKGIDLDIRDREFVVFVGPSGCGKSTLLRLIAGLEEVSSGRI 60

Query: 61  SIDGKKINDIEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNEISEL 120
            +DG+ I D+ P  RD+AMVFQ+YALYPHMTV +NM F L L      E+ +++   +  
Sbjct: 61  ELDGRDITDVSPAKRDLAMVFQTYALYPHMTVRKNMSFALDLAGADKQEVARKIEAAART 120

Query: 121 LQIKHLLDRKPKELSGGQRQRVALGRALS----RQTPVILFDEPLSNLDAHLRSQMRLEI 176
           L+++ LL+RKP++LSGGQRQRVA+GRA+     R   V LFDEPLSNLDA LR QMRLE+
Sbjct: 121 LELEPLLERKPRQLSGGQRQRVAIGRAIGRAIVRNPKVFLFDEPLSNLDAALRVQMRLEL 180

Query: 177 KRLHHNSKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGS 236
            RLH   ++TMIYVTHDQ+EA TL D++ VL  G IEQ+G+P E+YH P N F+A F+G+
Sbjct: 181 SRLHQELQATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPMELYHHPANLFVAGFLGT 240

Query: 237 PEMNFLEG------------------AVLEKIPWPEARKADQI-LGIRPDAFALNQGPLG 277
           P+M FL+G                   +   +     +  D + LGIRP+   LN+G  G
Sbjct: 241 PKMGFLKGHASRVEASGCEVELDAGCRLFLPVSGATLKAGDPVTLGIRPE--HLNRGSEG 298

Query: 278 TQEVALGDFQIDISENLGGQQMLHGTLAGNNVRILVDSMDNFSMK--QTLPLKIDLTKAH 335
             ++ +   + D+SE LG     H  +  N  ++ +    +F+ +  ++L L ++    H
Sbjct: 299 NCQLTV---KADVSERLGSDTYCH-VVTRNGEQLTMRIRGDFTPRYGESLSLTLEAAHCH 354

Query: 336 LFD 338
           LFD
Sbjct: 355 LFD 357


Lambda     K      H
   0.318    0.136    0.383 

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: 334
Number of extensions: 11
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: 347
Length of database: 371
Length adjustment: 29
Effective length of query: 318
Effective length of database: 342
Effective search space:   108756
Effective search space used:   108756
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: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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