GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Thiothrix lacustris DSM 21227

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate WP_028488026.1 Q394_RS0103345 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>NCBI__GCF_000621325.1:WP_028488026.1
          Length = 351

 Score =  323 bits (827), Expect = 6e-93
 Identities = 167/345 (48%), Positives = 226/345 (65%), Gaps = 7/345 (2%)

Query: 15  GWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGHEI 74
           G+AA+     L P++F RR     DV + +LFCGVCHSD H   N+W  + YP+VPGHEI
Sbjct: 7   GYAAQSAQDNLEPYRFERREPRADDVVIDILFCGVCHSDLHQARNDWANSVYPVVPGHEI 66

Query: 75  VGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCEN--TIDTYGSIYFDGT 132
           +G V  VGS V + K GD VG+GC+V SC+ CE C    E +C    T    G+   D  
Sbjct: 67  IGRVISVGSSVTRFKAGDQVGVGCMVDSCQHCEPCHHGLEQYCVEFPTFTYNGTDRHDHA 126

Query: 133 MTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVGL 192
            T+GGYS+ ++  + F+L+ P  L L   APLLCAGITTYSPL+++ + K G+K+ VVGL
Sbjct: 127 PTYGGYSEKIIVSDKFVLKVPDGLDLAGAAPLLCAGITTYSPLRHWKVGK-GSKVAVVGL 185

Query: 193 GGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDGII 252
           GGLGH+A+K+AKA GA+VT+   S  K ++A  +LGAD+ ++++D  QM    S  D II
Sbjct: 186 GGLGHMALKLAKALGAEVTLFTRSADKEQDA-RRLGADNIVISTDDAQMAAVNSRFDLII 244

Query: 253 DTVPVNHPLAPLFDLLKPNGKLVMVG--APEKPFELPVFSLLKGRKLLGGTINGGIKETQ 310
           DTVP  H + P    L  +G LV+VG   P  PF L    L+ GRK + G++ GGI ETQ
Sbjct: 245 DTVPYVHDINPYMPTLNISGTLVLVGYLGPLDPF-LNSAPLVLGRKSVAGSLIGGIAETQ 303

Query: 311 EMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDIAN 355
           EMLDF  +H IT+D+EVI +  +N A ER++KSDV+YRFVID+A+
Sbjct: 304 EMLDFCGEHGITSDIEVIKIQEINEAYERMLKSDVKYRFVIDMAS 348


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: 341
Number of extensions: 19
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: 351
Length adjustment: 29
Effective length of query: 336
Effective length of database: 322
Effective search space:   108192
Effective search space used:   108192
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 Apr 09 2024. 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