GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Phaeobacter inhibens BS107

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate GFF262 PGA1_c02740 sn-glycerol-3-phosphate import ATP-binding protein UgbC

Query= reanno::WCS417:GFF4321
         (386 letters)



>FitnessBrowser__Phaeo:GFF262
          Length = 348

 Score =  322 bits (824), Expect = 1e-92
 Identities = 175/364 (48%), Positives = 240/364 (65%), Gaps = 17/364 (4%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           MA + L +V K Y  G+ + + +    I++GEF++LVGPSGCGKSTL+  IAGLE IT G
Sbjct: 1   MAQVTLNSVRKVYPNGV-EAVTSSSFKIEDGEFVVLVGPSGCGKSTLLRMIAGLEDITEG 59

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            + IGD+ V+ + P DRDIAMVFQ+YALYP M+VR+NI +GLK RK P+A+I  +VA  A
Sbjct: 60  TLEIGDRVVNNVDPADRDIAMVFQNYALYPHMTVRKNIAYGLKNRKTPEAEIKQKVAEAA 119

Query: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           K+L +E  L+RKP QLSGGQ+QRVAMGRA+ R P ++LFDEPLSNLDAKLR +MR E+K 
Sbjct: 120 KMLNLEEYLDRKPSQLSGGQRQRVAMGRAIVRDPALFLFDEPLSNLDAKLRNQMRIEIKA 179

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240
           + +RL  T++YVTHDQ+EAMT+ D++ V+  G I+Q GTP EIY+NPA+ FVASF+G+PP
Sbjct: 180 LQRRLGVTSIYVTHDQVEAMTMADRIIVLNGGRIEQIGTPSEIYHNPASVFVASFMGAPP 239

Query: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300
           MN +   +      L   +  G      AL+T+  G     V LG+RPE + L A  G  
Sbjct: 240 MNLLDATIANGQVTLPDGVSMG------ALDTSAQGA----VKLGIRPEDVQLVAEGG-- 287

Query: 301 ASSIRAEVQVTEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFDAN 360
              +  +V++ E  G   L+  +L        +  D+    G T  +  DP+ + LFDA 
Sbjct: 288 ---LAIDVELIEELGAHRLLHGKLGGQPFTIHVLKDIPVDPG-THQISVDPAAICLFDAE 343

Query: 361 TGER 364
           +G+R
Sbjct: 344 SGQR 347


Lambda     K      H
   0.318    0.135    0.382 

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: 388
Number of extensions: 18
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: 386
Length of database: 348
Length adjustment: 30
Effective length of query: 356
Effective length of database: 318
Effective search space:   113208
Effective search space used:   113208
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 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