GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Desulfatiglans anilini DSM 4660

Align Leucine-, isoleucine-, valine-, threonine-, and alanine-binding protein; LIVAT-BP; Leu/Ile/Val/Thr/Ala-binding protein (characterized)
to candidate WP_028321169.1 H567_RS0109120 branched-chain amino acid ABC transporter substrate-binding protein

Query= SwissProt::P21175
         (373 letters)



>NCBI__GCF_000422285.1:WP_028321169.1
          Length = 386

 Score =  165 bits (418), Expect = 2e-45
 Identities = 115/343 (33%), Positives = 173/343 (50%), Gaps = 20/343 (5%)

Query: 30  IKIALAGPVTGPVAQYGDMQRAGALMAIEQINKAGGVNGAQLEGVIYDDACDPKQAVAVA 89
           +KI +   +TG  A  G     GA MA+++    G + G  +   + DD C    +V +A
Sbjct: 39  VKIGMGTMLTGDYAGMGIDIMHGAEMAVKE---KGLILGHPVILQVEDDGCAGPPSVVIA 95

Query: 90  NKVVNDG-VKFVVGHVCSSSTQPATDIYEDEGVLMITPSATAPEITSRGYKLIFRTIGLD 148
            K  ND  +  VVG++CS  ++PA+DI+    ++MI+PS+TA E+TSR   + FRT   D
Sbjct: 96  EKFCNDPLIAGVVGYMCSGGSKPASDIHNKYKMVMISPSSTALELTSRKIPIFFRTCWND 155

Query: 149 NMQGPVAGKFIAERYKDKTIAVLHDKQQYGEGIATEVKKTVEDAGIKVAVFEGLNAGDKD 208
            +Q   A  F A R   +  AVLHDK  YG+ +A +  + +E  G +V   EG+  GDKD
Sbjct: 156 RIQAQRAADFAASRGWLRA-AVLHDKSDYGQSLAEDFAQHLETRGGEVLAMEGVTRGDKD 214

Query: 209 FNALISKLKKAGVQFVYFGGYHPEMGLLLRQAKQAGLDARFMGPEG-VGNSEITAIAGDA 267
           F+ +++K+K    Q VYFGG   E  L++RQ ++ G+ A+F+  +G     +     G A
Sbjct: 215 FSPVLTKIKPLRPQLVYFGGMSAEGVLVVRQMQRVGIRAKFLSDDGCFTEKDFIQAGGRA 274

Query: 268 SEGMLATLPRAFEQDPKNKALIDAFKAKNQDPSGIFVLPAYSAVTVIAKGIEKAGEADPE 327
           + G   T   A E DP   A  ++       P   F   AY A T++   +E A E  P+
Sbjct: 275 ATGSFVTY--AQEPDPAWVAHFESM----YGPRQTFSPQAYDAATILLMAVESAAERQPD 328

Query: 328 --------KVAEALRANTFETPTGNLGFDEKGDLKNFDFTVYE 362
                   ++ +AL A   E  TG + FD  GD       VYE
Sbjct: 329 DSLLIDKRRLRDALAATDHEGVTGRIVFDTNGDRTGSVVAVYE 371


Lambda     K      H
   0.316    0.133    0.377 

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: 338
Number of extensions: 18
Number of successful extensions: 3
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: 373
Length of database: 386
Length adjustment: 30
Effective length of query: 343
Effective length of database: 356
Effective search space:   122108
Effective search space used:   122108
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 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