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:

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