GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Rhizobium johnstonii 3841

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_011652369.1 RL_RS14695 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_000009265.1:WP_011652369.1
          Length = 294

 Score =  171 bits (432), Expect = 2e-47
 Identities = 107/305 (35%), Positives = 175/305 (57%), Gaps = 18/305 (5%)

Query: 7   FFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAI-AGLAMMGL 65
           F Q L++GL  GS YAL AIG+T+++     +NFA GE  M+ ++   +A+ AGL M   
Sbjct: 4   FLQVLMSGLATGSIYALAAIGFTLLWQAAQTVNFAQGEFVMLPAFFMLMALGAGLPM--- 60

Query: 66  DSVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNR---LIPLISAIGMSIFLQNTVL 122
              PL +  A  AS+ V    GY  +R+   P++ S     L  +I+ + ++I L+ +V 
Sbjct: 61  ---PLAILVALAASVFVL---GYLFKRLIVEPMQASKAGGGLPLVIATMALAILLKESVK 114

Query: 123 LSQDSKDKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRA 182
               ++ +  P L+ G    G       +IS   I    ++L  ++ LTLF++R+R GRA
Sbjct: 115 EFYGAEAQPFPELVSG----GSLNVFGAVISVTDIAHLFISLAVVVALTLFLNRTRTGRA 170

Query: 183 CRACAEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAF 242
            +A A++  +A +LG++T  ++  TF+I AALA++A+ L++  Y     N  +L GL AF
Sbjct: 171 MQATAQNPNVAEILGVDTRRMVLYTFLINAALASLASFLITPFYLAKFSNGEYL-GLIAF 229

Query: 243 TAAVLGGIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGRP 302
            AA++GG   I GA++GGL++GV +   A     +Y+  V   LL++++L+RP G+LG P
Sbjct: 230 IAAIVGGFNQIRGALVGGLLIGVLDNMTATYVTAEYRAAVPLVLLIVIILWRPEGLLGTP 289

Query: 303 EVEKV 307
           E  KV
Sbjct: 290 EGRKV 294


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: 230
Number of extensions: 15
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: 307
Length of database: 294
Length adjustment: 27
Effective length of query: 280
Effective length of database: 267
Effective search space:    74760
Effective search space used:    74760
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 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