GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Rhodopseudomonas palustris CGA009

Align Branched-chain amino acid ABC transporter permease LivH; SubName: Full=Branched-chain amino acid transporter permease subunit LivH; SubName: Full=L-leucine ABC transporter membrane protein /L-isoleucine ABC transporter membrane protein /L-valine ABC transporter membrane protein (characterized, see rationale)
to candidate WP_011159344.1 TX73_RS19425 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_000195775.1:WP_011159344.1
          Length = 305

 Score =  318 bits (815), Expect = 1e-91
 Identities = 158/303 (52%), Positives = 221/303 (72%), Gaps = 1/303 (0%)

Query: 6   HFFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGL 65
           +F QQL+NGL +GS Y LIAIGYTMVYGI+GMINFAHG+++MIG ++A I+   L   GL
Sbjct: 3   YFAQQLINGLVLGSIYGLIAIGYTMVYGIVGMINFAHGDIFMIGGFIALISFLILVSFGL 62

Query: 66  DSVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQ 125
             VPL++    + S+ +T+ YG+++ERIAYRPLR S RL P++SAIGMS  L N   +SQ
Sbjct: 63  TFVPLILLVVLLVSMAITALYGWTVERIAYRPLRHSFRLAPMLSAIGMSFVLMNYAQVSQ 122

Query: 126 DSKDKSIPNLIPGNFAIGPGG-AHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACR 184
            ++ K +P +I G + +        V +S +QI+V V T+V +   T  ++++RLGR  R
Sbjct: 123 GARVKPVPPIITGGYTLHESADGFNVQLSNVQILVVVTTVVLLGIFTWLVAKTRLGRDMR 182

Query: 185 ACAEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTA 244
           AC +D  MA LLG++ +  I++TFVIGAALA++A ++  + YG+I+   GF+ G+KAFTA
Sbjct: 183 ACEQDQTMAALLGVDVDRTISMTFVIGAALASVAGMMYLLYYGLIDFFMGFIAGIKAFTA 242

Query: 245 AVLGGIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGRPEV 304
           AVLGGIGS+PGAMLGGL++G+ E F +  F  +YKDV AF +L++VL+F PTG+LGRPEV
Sbjct: 243 AVLGGIGSLPGAMLGGLLIGLIETFWSAYFSVEYKDVAAFSILIIVLIFMPTGLLGRPEV 302

Query: 305 EKV 307
           EKV
Sbjct: 303 EKV 305


Lambda     K      H
   0.327    0.144    0.411 

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: 353
Number of extensions: 10
Number of successful extensions: 2
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: 307
Length of database: 305
Length adjustment: 27
Effective length of query: 280
Effective length of database: 278
Effective search space:    77840
Effective search space used:    77840
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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