GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Bradyrhizobium sp. BTAi1

Align MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized)
to candidate WP_041750694.1 BBTA_RS16625 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::Q00752
         (377 letters)



>NCBI__GCF_000015165.1:WP_041750694.1
          Length = 353

 Score =  328 bits (841), Expect = 1e-94
 Identities = 185/351 (52%), Positives = 235/351 (66%), Gaps = 29/351 (8%)

Query: 26  LDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGELKIDGEVVNDKAPKDRDIAMVFQN 85
           + I++ EF+V VGPSGCGKST LRM+AGLE+IT G + I   VVN+  PK+RDIAMVFQN
Sbjct: 24  IPIEDGEFVVLVGPSGCGKSTLLRMLAGLENITSGTISIGERVVNNVQPKERDIAMVFQN 83

Query: 86  YALYPHMSVYDNMAFGLKLRHYSKEAIDKRVKEAAQILGLTEFLERKPADLSGGQRQRVA 145
           YALYPHM+V DNM F LKLR    E I K V  AA+IL LT  L+R P  LSGGQRQRVA
Sbjct: 84  YALYPHMTVADNMGFSLKLRGARPEDIKKGVARAAEILALTPLLDRYPRQLSGGQRQRVA 143

Query: 146 MGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEIAKIHRRIGATTIYVTHDQTEAMTLADR 205
           MGRAIVRD +VFL DEPLSNLDAKLRV+MR EI ++H+R+  TT+YVTHDQ EAMT+AD+
Sbjct: 144 MGRAIVRDPQVFLFDEPLSNLDAKLRVAMRTEIKELHQRLKTTTVYVTHDQIEAMTMADK 203

Query: 206 IVIMSSTKNEDGSGTIGRVEQVGTPQELYNRPANKFVAGFIGSPAMNFFDVTIKDGHLVS 265
           IV+M            G VEQ+G+P +LY++P N+FVAGFIGSPAMNF      +GHL S
Sbjct: 204 IVVMHD----------GIVEQMGSPLDLYDKPDNQFVAGFIGSPAMNFL-----NGHLKS 248

Query: 266 KDGLTIAVTEG-QLKMLESKGFKN-KNLIFGIRPEDISSSLLVQETYPDATVDAEVVVSE 323
              + +    G +L +L +    N + +++G+RPE +  +        D  ++AEVVV E
Sbjct: 249 NGTVYVETDNGAKLPLLTAPAASNGRPVVYGVRPEHLELA--------DDGIEAEVVVVE 300

Query: 324 LLGSETMLYLKLGQTEFAARVDARDFHE--PGEKVSLTFNVAKGHFFDAET 372
             GSET +  ++G  +  A    RD HE  PG K+ L    +  H FD +T
Sbjct: 301 PTGSETQIVARIGTQDIIAVF--RDRHEVVPGAKIHLRPRASAAHLFDKDT 349


Lambda     K      H
   0.318    0.135    0.375 

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: 377
Number of extensions: 17
Number of successful extensions: 3
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: 377
Length of database: 353
Length adjustment: 30
Effective length of query: 347
Effective length of database: 323
Effective search space:   112081
Effective search space used:   112081
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