GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araV in Jannaschia aquimarina GSW-M26

Align AraV, component of Arabinose, fructose, xylose porter (characterized)
to candidate WP_043916916.1 jaqu_RS00215 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::Q97UF2
         (371 letters)



>NCBI__GCF_000877395.1:WP_043916916.1
          Length = 372

 Score =  196 bits (497), Expect = 1e-54
 Identities = 132/390 (33%), Positives = 223/390 (57%), Gaps = 47/390 (12%)

Query: 1   MTTIRVENLSKIFKKGKTEVKAVDNVSITIDSGMAFGVLGPSGHGKTTFLRLIAGLEEPT 60
           M  +++++++K++     +V+ + ++ + I++G     +GPSG GK+T LR+IAGLE+ +
Sbjct: 1   MANLKLKDVAKVYGG---QVEVLKDIDLDIETGELIVFVGPSGCGKSTLLRMIAGLEQIS 57

Query: 61  SGYIYFDNEAVSSPRRVMMSPEKRGIAMVFQNWALYPNMTVFDNIAFPLKLAKVPKDKIE 120
            G +  D   V+      + P +RGIAMVFQ++ALYP+MTV+DN+AF L++AK  K++I+
Sbjct: 58  GGTLEIDGMVVND-----VPPSERGIAMVFQSYALYPHMTVYDNMAFALQIAKKSKEEID 112

Query: 121 NKVKEVSEELGLSGVLNRYPKELSGGQMQRTAIARALVKDPKVLLLDEPFSNLDAQIRES 180
             V+  +++L L+  L+R PK LSGGQ QR AI R++V+DPKV L DEP SNLDA +R +
Sbjct: 113 RAVRAAADKLQLTEYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVA 172

Query: 181 ARALVRKIQRERKLTTLI-VSHDPADIFAIANKAGVI----VNG---KFAQIGTPTEIYE 232
            R  + +++ +   +T+I V+HD  +   +A++  V+     NG     AQ+GTP E+YE
Sbjct: 173 TRIEIAQLKEQMPDSTMIYVTHDQVEAMTLASRIVVLDALKDNGYKYSIAQVGTPLELYE 232

Query: 233 YPATDLIARLTGE--INLIQAKII---ENNAIIANL-------KVPLNNMELKGQSNIVI 280
            P ++ +AR  G   +NL++ +I+   E   +   L        VP +  E +G + + +
Sbjct: 233 TPNSEFVARFIGSPAMNLLEGEIVATGETTTLRTRLGAGTITSNVP-SRPEDQG-AQVKV 290

Query: 281 GLRPDDLTLSDT-------LLDKYIDMGIVKVKLVSYGAGIFKIVVSPITDENIDIIVDA 333
           G+RP+D   +D+        ++    +G V +     GAG    V++ +           
Sbjct: 291 GIRPEDAVATDSEDFAFSGKVEVEERLGEVTLLYFERGAGQNDPVIAKL---------PG 341

Query: 334 EEPLETGIETHLLAKPNKVKIFDLNGSNLI 363
             P   G    L A P KV IF  +G++L+
Sbjct: 342 IHPGMRGNTVKLTADPAKVHIFQ-DGTSLL 370


Lambda     K      H
   0.317    0.136    0.374 

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: 306
Number of extensions: 11
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: 371
Length of database: 372
Length adjustment: 30
Effective length of query: 341
Effective length of database: 342
Effective search space:   116622
Effective search space used:   116622
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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