GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Phaeobacter inhibens BS107

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate GFF1915 PGA1_c19470 ABC transporter, ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Phaeo:GFF1915
          Length = 363

 Score =  282 bits (721), Expect = 1e-80
 Identities = 161/368 (43%), Positives = 224/368 (60%), Gaps = 21/368 (5%)

Query: 4   IQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDIYIG 63
           +   DL+ RFG    +  L+LDI   EFLVL+G SGCGKST L  +AGL+  T G I+I 
Sbjct: 13  VSARDLSVRFGAVEVLKSLNLDIQKGEFLVLLGASGCGKSTLLNTIAGLQEATEGQIWIN 72

Query: 64  GDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAETLG 123
            +++ +R P++R +AMVFQ YALYP MTVR N+ FGL   +    AE D+ V E A  L 
Sbjct: 73  DENVTWREPKDRGLAMVFQSYALYPKMTVRGNLAFGLRMNK-VPKAEADKLVDEAARVLQ 131

Query: 124 IADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNLQDQ 183
           + +LLDR+P ELSGGQ+QRVA+GRA+VR  +VFL DEPLSNLDAKLRAE+R EL+ L  +
Sbjct: 132 LEELLDRRPGELSGGQRQRVAIGRALVRKVDVFLFDEPLSNLDAKLRAELRVELKRLHQE 191

Query: 184 LAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMINLV 243
           L  T +YVTH+Q EA+T+ADRIAVM DG +QQ+ SP E Y  P N +VA+F+G P +N V
Sbjct: 192 LGATMIYVTHDQVEALTLADRIAVMKDGVVQQLDSPEEIYRRPANRYVAQFVGLPSMNFV 251

Query: 244 RGTRSESTFV-GEHFSYPLDE-DVMESVDDRDDFVLGVRPEDIEVADAAPDDAALDDHDL 301
            G  +ES  +  E F   LD+ ++  +     +  +G+RPE +  A+A            
Sbjct: 252 NGVVTESGAIQTEDFELALDQCNLASTPAPGTEVEIGIRPEHVHPANAG---------GF 302

Query: 302 QMDVTVVEPHGDQNVL--HLSHPDQPSADDALQAVTEGMHLVTRGDRVTVTIPPDKIHLF 359
            +DV +VE  G + ++   + +      DD    +         GD+V + + P    +F
Sbjct: 303 MLDVGMVELLGSERLIWGKVGNTSIVMRDDPDTTIRS-------GDQVRINLKPGAFSVF 355

Query: 360 DAETGTAV 367
            A+TG  +
Sbjct: 356 SAKTGLRI 363


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: 329
Number of extensions: 15
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: 383
Length of database: 363
Length adjustment: 30
Effective length of query: 353
Effective length of database: 333
Effective search space:   117549
Effective search space used:   117549
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 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