GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Nafulsella turpanensis ZLM-10

Align alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71) (characterized)
to candidate WP_017732869.1 F752_RS0116570 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::Q8H0L8
         (359 letters)



>NCBI__GCF_000346615.1:WP_017732869.1
          Length = 347

 Score =  348 bits (893), Expect = e-100
 Identities = 174/343 (50%), Positives = 237/343 (69%), Gaps = 5/343 (1%)

Query: 15  GWATRHTSGVLSPFNFSRRVTGEKHVQFKVMYCGICHSDLHQLKNEWGNTKYPMVPGHEV 74
           G+A +     L+PF F RR      VQ ++MYCG+CHSDLH  +NEWG T YP +PGHE+
Sbjct: 6   GYAAQAADQPLAPFTFERRALRPHDVQIEIMYCGVCHSDLHTARNEWGGTVYPCIPGHEI 65

Query: 75  VGVVIEVGSKVEKFKVGDKVGVGCMVGSCRKCENCTVDLENYCP-RQIPTYNGYS-LDGT 132
           VG +  VGS+V KFKVG+  GVGC+V SCR+C NC   LE YC      TYN    +DGT
Sbjct: 66  VGRITNVGSEVTKFKVGELTGVGCLVDSCRECSNCQQGLEQYCEVGNTWTYNSPDPVDGT 125

Query: 133 LTFGGYSDMMVSDEHFVVRWPENLSMD-AAPLLCAGITTYSPLKYFGLDKPGMHIGVVGL 191
            T+GGYS  +V D+ FV+   + L ++  APLLCAGITTYSPL+++ + K G  + V+GL
Sbjct: 126 NTYGGYSKQIVVDQDFVLLISDRLPLEGVAPLLCAGITTYSPLRHWKVGK-GHKVAVLGL 184

Query: 192 GGLGHMAVKFAKAFGTKVTVISTSANKKQEAIERLGADSFLISRDPEQMKAAMNTLDGII 251
           GGLGHMAVKFA +FG +VT++STS +K+++A  RLGA  F +++DP Q+KA  N  D I+
Sbjct: 185 GGLGHMAVKFAASFGAEVTMLSTSPSKEEDA-RRLGASHFALTKDPAQVKALTNQFDFIV 243

Query: 252 DTVSAVHPILPLLMLMKSHGKLVMVGAPEKPVELPVFPLLMGRKLVAGSCIGGMKETQEM 311
           +TVSA H     L ++K+ G ++ VG P +P ++    L+  R+ V GS IGG+ ETQEM
Sbjct: 244 NTVSAPHDYNMYLKMLKTSGTMICVGVPPEPSKIIGGYLIGNRRSVGGSLIGGLPETQEM 303

Query: 312 LDFAAKHNITPDIEVVPMDYVNTALERLLKSDVKYRFVLDIGN 354
           LD+ A+HNI  D+EV+ M Y+N A ER+LK DV+YRFV+D+ +
Sbjct: 304 LDYCAEHNIVSDVEVIDMSYINEAYERMLKGDVRYRFVIDMAS 346


Lambda     K      H
   0.320    0.137    0.417 

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: 371
Number of extensions: 17
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: 359
Length of database: 347
Length adjustment: 29
Effective length of query: 330
Effective length of database: 318
Effective search space:   104940
Effective search space used:   104940
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 (21.8 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