Aligments for a candidate for rbsA in Shewanella loihica PV-4

GapMind for catabolism of small carbon sources

Aligments for a candidate for rbsA in Shewanella loihica PV-4

Align Ribose import ATP-binding protein RbsA 2, component of D-ribose porter (Nanavati et al., 2006). Induced by ribose (characterized)
to candidate 5208462 Shew_0974 spermidine/putrescine ABC transporter ATPase subunit (RefSeq)

Query= TCDB::Q9X051
         (523 letters)



>FitnessBrowser__PV4:5208462
          Length = 378

 Score =  121 bits (303), Expect = 5e-32
 Identities = 87/271 (32%), Positives = 149/271 (54%), Gaps = 21/271 (7%)

Query: 5   TEKEREVLLEARNITKTFPGVIAVNNVTLQIYKGEVCALVGENGAGKSTLMKILAGVYPD 64
           T+ + EVLL+   ++K F  V AV++V+L I +GE+ AL+G +G+GKSTL+++LAG    
Sbjct: 13  TKTQGEVLLKIERVSKLFDDVRAVDDVSLNINRGEIFALLGGSGSGKSTLLRMLAGFEKP 72

Query: 65  YEGQIFLEGKEVRFRNPREAQENGIALIPQELDLVPNLSSAENIFLSREPVNEFGVIEYQ 124
            EG+I+L+G+++    P    E  I ++ Q   L P+++ A+NI         FG ++  
Sbjct: 73  TEGRIYLDGQDITDMPP---YERPINMMFQSYALFPHMTVAQNI--------AFG-LKQD 120

Query: 125 KM----FEQASKLFSKLGVNIDP--KTKVEDLSTSQQQMVAIAKALSLDAKIIIMDEPTS 178
           KM     EQ  K   KL V+++P  K K   LS  Q+Q VA+A++L+   K++++DEP  
Sbjct: 121 KMPKAEIEQRVKEMLKL-VHMEPYAKRKPNQLSGGQRQRVALARSLAKRPKLLLLDEPMG 179

Query: 179 AIGKR-ETEQLFNIIRSLKNEGKSVIYISHRLEEIFEIADRVVVMRDGRKVGEGPIEEFD 237
           A+ K+  T+    ++  L+  G + + ++H  EE   +A+R+ +M DG     G   +  
Sbjct: 180 ALDKKLRTQMQLEVVDILEAVGVTCVMVTHDQEEAMTMAERIAIMNDGWIAQTGSPMDI- 238

Query: 238 HDKLVRLMVGRSIDQFFIKERATITDEIFRV 268
           ++     MV   I    + E   + DE+  V
Sbjct: 239 YESPANRMVAEFIGSVNLFEGDIVEDEVDHV 269



 Score = 88.6 bits (218), Expect = 4e-22
 Identities = 64/211 (30%), Positives = 111/211 (52%), Gaps = 23/211 (10%)

Query: 283 VDDVSFYVRKGEVLGIYGLVGAGRTELLEAIFGAHPGRTEGKVFIGGKEIKIHSPRDAVK 342
           VDDVS  + +GE+  + G  G+G++ LL  + G     TEG++++ G++I    P +   
Sbjct: 36  VDDVSLNINRGEIFALLGGSGSGKSTLLRMLAGFEKP-TEGRIYLDGQDITDMPPYERPI 94

Query: 343 NGIGLVPEDRKTAGLILQMSVLHNITLPSVVMKLIVRKFGLIDSQLEK-EIVRSFIEKLN 401
           N +       ++  L   M+V  NI             FGL   ++ K EI +   E L 
Sbjct: 95  NMMF------QSYALFPHMTVAQNIA------------FGLKQDKMPKAEIEQRVKEMLK 136

Query: 402 IKTPSPY--QIVENLSGGNQQKVVLAKWLAIKPKVLLLDEPTRGIDVNAKSEI-YKLISE 458
           +    PY  +    LSGG +Q+V LA+ LA +PK+LLLDEP   +D   ++++  +++  
Sbjct: 137 LVHMEPYAKRKPNQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRTQMQLEVVDI 196

Query: 459 MAVSGMGVVMVSSELPEILAMSDRILVMSEG 489
           +   G+  VMV+ +  E + M++RI +M++G
Sbjct: 197 LEAVGVTCVMVTHDQEEAMTMAERIAIMNDG 227


Lambda     K      H
   0.317    0.137    0.372 

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: 406
Number of extensions: 22
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 523
Length of database: 378
Length adjustment: 32
Effective length of query: 491
Effective length of database: 346
Effective search space:   169886
Effective search space used:   169886
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: 51 (24.3 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources