GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Neptunomonas antarctica S3-22

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate WP_054340851.1 Nant_RS06010 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>NCBI__GCF_001305295.1:WP_054340851.1
          Length = 349

 Score =  325 bits (833), Expect = 1e-93
 Identities = 165/342 (48%), Positives = 232/342 (67%), Gaps = 7/342 (2%)

Query: 16  WAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGHEIV 75
           +AA+  T  ++P    RR     DV + +L+CGVCHSD H   N+WG + YP+VPGHEI+
Sbjct: 5   YAAQTATSKMAPLNIQRRTLRPDDVAIDILYCGVCHSDIHQAENDWGNSIYPVVPGHEII 64

Query: 76  GVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCEN-TIDTY-GSIYFDGTM 133
           G VT +G  V + KVGD VG+GC+V SC SC SC    E +CEN  + TY G  Y+DGT+
Sbjct: 65  GRVTSIGPNVTQYKVGDIVGVGCMVDSCCSCSSCHAGLEQYCENGMVGTYNGKDYYDGTL 124

Query: 134 THGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVGLG 193
           T GGYS+ +V  E F+L  P  L + + APLLCAGITTYSPLK+YG+ K G K+G++G+G
Sbjct: 125 TSGGYSEHIVVREAFVLSIPDTLDIKAAAPLLCAGITTYSPLKHYGV-KAGDKVGILGMG 183

Query: 194 GLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDGIID 253
           GLGH+ VK AKA GA+VTV   S+SK  EA + LGAD  ++++D +QM  A  + + ++D
Sbjct: 184 GLGHMGVKYAKALGAEVTVFTRSQSKVAEA-KLLGADHVIVSTDADQMAAATLTFNFLLD 242

Query: 254 TVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELPVF--SLLKGRKLLGGTINGGIKETQE 311
           T+PV H   P  + LK +G  ++VG      + P++  SL+  R++L G++ GGI ETQE
Sbjct: 243 TIPVAHDFNPYLNCLKVDGAHIIVGL-VTGIDPPIWGASLITKRRILAGSMIGGIAETQE 301

Query: 312 MLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDI 353
           ML+F+A+H I  +VE++ +  +N A ER+ K DV+YRFVID+
Sbjct: 302 MLNFSAEHGINCEVEMLDIQNINVAYERMKKGDVKYRFVIDM 343


Lambda     K      H
   0.319    0.137    0.415 

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: 368
Number of extensions: 25
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: 365
Length of database: 349
Length adjustment: 29
Effective length of query: 336
Effective length of database: 320
Effective search space:   107520
Effective search space used:   107520
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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 24 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