GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Magnetovibrio blakemorei MV-1

Align ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate WP_069957743.1 BEN30_RS07675 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8DQI0
         (292 letters)



>NCBI__GCF_001746755.1:WP_069957743.1
          Length = 338

 Score =  134 bits (338), Expect = 2e-36
 Identities = 98/337 (29%), Positives = 166/337 (49%), Gaps = 56/337 (16%)

Query: 1   MNLMLQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFIGYFL------- 53
           M+ ++ Q++NGL  G  YAL+ALG T+ +G + ++NFAHG ++MMGAF    +       
Sbjct: 1   MDAIVIQILNGLDKGGAYALIALGLTLAFGTLGIVNFAHGALFMMGAFCAVTVQKLLTIS 60

Query: 54  --INSFQMNFFVA--------------------------LIVAMLATAILGVVIEFLAYR 85
             +    + FF A                          +++A+   A++GVV+E    R
Sbjct: 61  ARVRDMSVTFFEAYKETPYLELWWGDTGTTIIEYSVPLSILIAIPVMALVGVVMERGLIR 120

Query: 86  PLRHSTRIAVLITAIGVSFLLEYGMVYLVGANTRAFPQAIQTV---RYDLGPISLTNVQL 142
                T    ++   G++ +++  + +  GAN    PQAI  +     ++G +   +  L
Sbjct: 121 FFYKRTHAEQILVTFGLAIVIQEIIRHFFGANP--IPQAIPEIVSGSANVGTMLGLSDTL 178

Query: 143 MILGISLILMILLQVIV-------QKTKMGKAMRAVSVDSDAAQLMGINVNRTISFTFAL 195
           +     LI      V++       Q T  G  +RA   D D   L+GIN+ R  +  FAL
Sbjct: 179 VYPWWRLIYFCFATVVIGGVFAFLQYTTYGMVVRAGMADRDTVGLLGINIQRRFTIVFAL 238

Query: 196 GSALAGAAGVLIALYYNSLEP--LMGVTPGLKSFVAAVLGGIGIIPGAALGGFVIGLLET 253
            + +AG AGV+   Y   L P   MG+   + SFV  V+GG+G +PGA   GF++G+L++
Sbjct: 239 AAVVAGLAGVM---YTPVLPPDYHMGMDFLVLSFVVVVVGGMGSLPGAVAAGFLLGILQS 295

Query: 254 FATAFGMSDF----RDAIVYGILLLILIVRPAGILGK 286
           FA+   +  F       I+Y + ++I++VRP G++G+
Sbjct: 296 FASMNEIKQFLPGIDQIIIYLVAVVIILVRPRGLMGR 332


Lambda     K      H
   0.330    0.146    0.407 

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: 262
Number of extensions: 22
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 3
Length of query: 292
Length of database: 338
Length adjustment: 27
Effective length of query: 265
Effective length of database: 311
Effective search space:    82415
Effective search space used:    82415
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 (21.8 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