GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Klebsiella michiganensis M5al

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 BWI76_RS05990 BWI76_RS05990 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A0D9B2B6
         (307 letters)



>FitnessBrowser__Koxy:BWI76_RS05990
          Length = 299

 Score =  233 bits (595), Expect = 3e-66
 Identities = 128/304 (42%), Positives = 189/304 (62%), Gaps = 17/304 (5%)

Query: 7   FFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGLD 66
           F QQ+VNG+++G  YALIAIGYTMVYG++ +INFAH +V M+G++      +        
Sbjct: 6   FLQQVVNGMSLGGMYALIAIGYTMVYGVLRLINFAHADVMMVGAFTTLFLFS-------- 57

Query: 67  SVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQN--TVLLS 124
           S+ L    A   ++ +   +G  I+R+AYRPLR ++++  LI+AIG+S FL+N   VL  
Sbjct: 58  SIGLPFGVAVFLTLALCGLFGMLIDRVAYRPLRQASKISMLITAIGVSFFLENLFNVLFG 117

Query: 125 QDSKDKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACR 184
             S+  S P+      A G     +V+I+ +  +V ++T++ +L +   + R+R G A R
Sbjct: 118 GSSRFFSAPDFFNNTRAFG-----DVIITNVAWIVPLITVLLLLAILWLLYRTRYGMAIR 172

Query: 185 ACAEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTA 244
           A A D+    L+GI+ N II+L F +G++LAA+  V  S+ Y  I+P  G L+GLKAF A
Sbjct: 173 AVAFDVNTVRLMGIDANRIISLVFALGSSLAALGGVFYSISYPTIDPLMGVLIGLKAFAA 232

Query: 245 AVLGGIGSIPGAMLGGLVLGVAEAFGADIFGD--QYKDVVAFGLLVLVLLFRPTGILGRP 302
           AVLGGIGS+ GA+LGG +LG  E     +F +   YKD  AF  L+LVLLFRP GI+G  
Sbjct: 233 AVLGGIGSVTGAVLGGFILGFTEVVAVALFPELGGYKDAFAFMFLILVLLFRPVGIMGDE 292

Query: 303 EVEK 306
            +E+
Sbjct: 293 RLER 296


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: 308
Number of extensions: 20
Number of successful extensions: 4
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: 299
Length adjustment: 27
Effective length of query: 280
Effective length of database: 272
Effective search space:    76160
Effective search space used:    76160
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 17 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