GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Bacteroides thetaiotaomicron VPI-5482

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 352338 BT2811 alkyl hydroperoxide reductase subunit F (NCBI ptt file)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Btheta:352338
          Length = 523

 Score =  171 bits (433), Expect = 4e-47
 Identities = 112/308 (36%), Positives = 174/308 (56%), Gaps = 14/308 (4%)

Query: 3   EVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTG 62
           EV+   VI+ G GPAG SAA+Y+AR  L+ + I   + GGQ+  T  ++N    V   TG
Sbjct: 214 EVKEYDVIVAGGGPAGVSAAIYSARKGLR-VAIVAERVGGQVKETVGIENLIS-VPETTG 271

Query: 63  PALMERMREHAERFETEIVFDH-INAVDFAAKPYTLTGD-SATYTCDALIIATGASARYL 120
             L + ++ H  R+  +++    I  V+ A K   +T      +   ALIIATGAS R L
Sbjct: 272 SELADNLKTHLLRYPVDLLEQRKIEKVELAGKDKLVTTSVGEKFIAPALIIATGASWRKL 331

Query: 121 GLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRET 180
            +P E  ++G+GV+ C  CDG FY+ K VAVVGGGN+ +E A+ LA I S VT+    + 
Sbjct: 332 NVPGENDYIGRGVAFCPHCDGPFYKGKQVAVVGGGNSGIEAAIDLAGICSKVTVFEFMDE 391

Query: 181 FRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNNDGSFDEL-KVDGVF 239
            +A+ +L ++L +      + + +++   EV+G+   +T  R+K+     + L ++DGVF
Sbjct: 392 LKADNVLQERLKSL---PNVEVFVSSQTTEVIGNGDKLTALRIKDRKTEEERLVELDGVF 448

Query: 240 IAIGHTPNTSLFEGQL-TLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSA 298
           + IG + N+S+F   + T + G +V+          T+V GI+AAGDV+   Y+Q I S 
Sbjct: 449 VQIGLSANSSVFRDIVETNRPGEIVIDA-----HCRTNVTGIYAAGDVSTVPYKQIIISM 503

Query: 299 GAGCMAAL 306
           G G  AAL
Sbjct: 504 GEGAKAAL 511


Lambda     K      H
   0.318    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: 417
Number of extensions: 24
Number of successful extensions: 5
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: 320
Length of database: 523
Length adjustment: 31
Effective length of query: 289
Effective length of database: 492
Effective search space:   142188
Effective search space used:   142188
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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