GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Herbaspirillum seropedicae SmR1

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate HSERO_RS01355 HSERO_RS01355 sugar ABC transporter ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__HerbieS:HSERO_RS01355
          Length = 381

 Score =  264 bits (674), Expect = 4e-75
 Identities = 165/376 (43%), Positives = 213/376 (56%), Gaps = 26/376 (6%)

Query: 1   MGQIQLTDLTKRFGDTVAV-DDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGD 59
           M  I L    K +GD   V  ++ LDI + EF V +GPSGCGKST LR +AGLE  TSGD
Sbjct: 1   MASITLRAAQKAYGDAPPVIRNVDLDIGEHEFCVFLGPSGCGKSTLLRSIAGLEDLTSGD 60

Query: 60  IYIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVA 119
           ++IGG  +N      R +AMVFQ YAL+PHMTV +N+ FGL   +    AE +++V E A
Sbjct: 61  LFIGGKRVNDVPSAQRSVAMVFQSYALFPHMTVYENMSFGLTLAK-LPKAEIEQKVREAA 119

Query: 120 ETLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQN 179
             L + +LL RKP ELSGGQ+QRVA+GRAIVR P VFL DEPLSNLDA LR++ R E+  
Sbjct: 120 RILQLEELLQRKPKELSGGQRQRVAIGRAIVRRPGVFLFDEPLSNLDATLRSQTRIEIAR 179

Query: 180 LQDQL-AVTTVYVTHNQTEAMTMADRIAVMDD-------GELQQVASPFECYHEPNNLFV 231
           L  Q    + VYVTH+Q EAMT+ADRI ++         G + QV +P E YH P N FV
Sbjct: 180 LHRQFEQASVVYVTHDQVEAMTLADRIVLLHAGADTQRFGSIAQVGTPMELYHHPRNRFV 239

Query: 232 AEFIGEPMINL----VRGTRSESTFVGEHFS-YPLDEDVMESVDDRDDFVLGVRPEDIEV 286
           A FIG P +N     V G +     V    S   L      ++       +GVRPE +E+
Sbjct: 240 AGFIGSPRMNFLPAQVAGVQENGILVRLSGSEETLLVAAQGALQPGQMVTVGVRPEHMEI 299

Query: 287 ADAAPDDAALDDHDLQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDR 346
                       + +  +V +VE  G+Q  +HL  P    A   L A   G   +TRG+R
Sbjct: 300 GSQG-------QYGIHREVVLVERLGEQTYVHLDEP----AGQPLVAKAAGDARITRGER 348

Query: 347 VTVTIPPDKIHLFDAE 362
           V V I P   +LFD +
Sbjct: 349 VRVAIAPACAYLFDQD 364


Lambda     K      H
   0.317    0.135    0.386 

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: 367
Number of extensions: 22
Number of successful extensions: 6
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: 383
Length of database: 381
Length adjustment: 30
Effective length of query: 353
Effective length of database: 351
Effective search space:   123903
Effective search space used:   123903
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 (21.6 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