GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Malonomonas rubra DSM 5091

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_072905065.1 BUB13_RS01980 branched-chain amino acid ABC transporter permease LivH

Query= uniprot:A0A0D9B2B6
         (307 letters)



>NCBI__GCF_900142125.1:WP_072905065.1
          Length = 300

 Score =  313 bits (802), Expect = 3e-90
 Identities = 169/302 (55%), Positives = 219/302 (72%), Gaps = 4/302 (1%)

Query: 6   HFFQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYVAFIAIAGLAMMGL 65
           +F +  + GLT GS YALIA+GYTMVYGII +INFAHGE+YMIG++VA I    L + G 
Sbjct: 3   YFLELFLGGLTRGSIYALIALGYTMVYGIIQLINFAHGEIYMIGAFVALIVAGILTIYGF 62

Query: 66  DSVPLLMTAAFIASIVVTSSYGYSIERIAYRPLRGSNRLIPLISAIGMSIFLQNTVLLSQ 125
             + +L+ AA IA+I+   +YGY++E+IAYRPLRG+ RL PLISAIGMSIFLQN VLL+Q
Sbjct: 63  AGISVLVLAA-IAAIIWACAYGYTLEKIAYRPLRGAPRLSPLISAIGMSIFLQNYVLLAQ 121

Query: 126 DSKDKSIPNLIPGNFAIGPGGAHEVLISYMQIVVFVVTLVAMLGLTLFISRSRLGRACRA 185
            S     PNLIP +F      AH  +I   ++V+ + T V M+ LTL I ++++G+A RA
Sbjct: 122 TSDFLPFPNLIP-DFEFMEPVAH--IIGSPELVILITTFVTMILLTLLIKKTKVGKAMRA 178

Query: 186 CAEDIKMANLLGINTNNIIALTFVIGAALAAIAAVLLSMQYGVINPNAGFLVGLKAFTAA 245
             +D+ MA L+GIN + II+LTF+IG+ALAAI  VL++   G +N   GFL G+KAFTAA
Sbjct: 179 TQQDMSMARLVGINVDRIISLTFIIGSALAAIGGVLVASYIGQVNFYIGFLAGVKAFTAA 238

Query: 246 VLGGIGSIPGAMLGGLVLGVAEAFGADIFGDQYKDVVAFGLLVLVLLFRPTGILGRPEVE 305
           VLGGIGSIPGA+LGGLVLG  E+F A      Y+DV AFGLLVL+L+ RP GILG+   +
Sbjct: 239 VLGGIGSIPGAVLGGLVLGWTESFAAGYVSSDYEDVFAFGLLVLILILRPAGILGKARKQ 298

Query: 306 KV 307
           KV
Sbjct: 299 KV 300


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: 328
Number of extensions: 17
Number of successful extensions: 5
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: 300
Length adjustment: 27
Effective length of query: 280
Effective length of database: 273
Effective search space:    76440
Effective search space used:    76440
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