GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Bacteroides thetaiotaomicron VPI-5482

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate 350819 BT1291 spermidine/putrescine transport ATP-binding protein (NCBI ptt file)

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Btheta:350819
          Length = 463

 Score =  229 bits (583), Expect = 2e-64
 Identities = 122/284 (42%), Positives = 183/284 (64%), Gaps = 7/284 (2%)

Query: 4   IQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDIYIG 63
           I+++ ++K FGD  A+DD++L++   EF+ ++GPSGCGK+T LR++AG +T + G+I I 
Sbjct: 10  IEVSHVSKFFGDKTALDDVTLNVKKGEFVTILGPSGCGKTTLLRLIAGFQTASEGEIRIS 69

Query: 64  GDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVA-ETL 122
           G  +    P  R +  VFQ YAL+PH+ V  NI FGL+ ++  T  +   + V+ A + +
Sbjct: 70  GKEITQTPPHKRPVNTVFQKYALFPHLNVYDNIAFGLKLKK--TPKQTIGKKVKAALKMV 127

Query: 123 GIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNLQD 182
           G+ D   R  D LSGGQQQRVA+ RAIV +PEV L+DEPL+ LD K+R +M+ EL+ +  
Sbjct: 128 GMTDYEYRDVDSLSGGQQQRVAIARAIVNEPEVLLLDEPLAALDLKMRKDMQMELKEMHK 187

Query: 183 QLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMINL 242
            L +T VYVTH+Q EA+T++D I VM +G++QQ+ +P + Y+EP N FVA+FIGE   N+
Sbjct: 188 SLGITFVYVTHDQEEALTLSDTIVVMSEGKIQQIGTPIDIYNEPINSFVADFIGES--NI 245

Query: 243 VRGTRSESTFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEV 286
           + GT      V   F     E V E   +     + +RPED+ +
Sbjct: 246 LNGTMIHDKLV--RFCGTEFECVDEGFGENTPVDVVIRPEDLYI 287



 Score = 25.8 bits (55), Expect = 0.003
 Identities = 10/15 (66%), Positives = 12/15 (80%)

Query: 344 GDRVTVTIPPDKIHL 358
           GDRV +TIPPD I +
Sbjct: 444 GDRVGITIPPDAIRV 458


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: 459
Number of extensions: 24
Number of successful extensions: 3
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: 383
Length of database: 463
Length adjustment: 32
Effective length of query: 351
Effective length of database: 431
Effective search space:   151281
Effective search space used:   151281
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