GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Rhizobium johnstonii 3841

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_011652368.1 RL_RS14690 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_000009265.1:WP_011652368.1
          Length = 337

 Score =  164 bits (416), Expect = 3e-45
 Identities = 102/319 (31%), Positives = 168/319 (52%), Gaps = 14/319 (4%)

Query: 88  KQKLFLVALLVLAVAWPFMVSRGTVDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYA 147
           K  L  V + +LA+A P         I    +IY I  +GLN+ +G +G + L    F A
Sbjct: 7   KWLLIAVGIALLALA-PIGHGNYVALILCSWLIYTIAAMGLNLTLGYAGQISLAQASFMA 65

Query: 148 IGAYTFALLNHYYGLGFWTCLPIAGLMAAAAGFLLGFPVLRLRGDYLAIVTLGFGEIVRI 207
           +GAY  AL+    G+ +   +P++       G L+GFP LR++G +LA VTL F  ++ +
Sbjct: 66  VGAYITALMT-MNGIHWLIAMPVSVAACFVIGLLVGFPALRVKGHFLAFVTLAFNTLLVL 124

Query: 208 LLLNNTEITGGPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIFLYLV 267
           +L N   +TGG  G S +P+P  +  +             S    +    + ++ +L LV
Sbjct: 125 VLRNEDWLTGGSYGKSNMPRPDFWVFDTGMK---------STVLSIPLTSNQKMYYLCLV 175

Query: 268 ALLLVVLSLFVINRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAG 327
             ++  L ++    L+R P GRA++ LRE+ I   SLGL  RRI L AF I +A  G AG
Sbjct: 176 VFVIFALLMY---GLVRSPWGRAFKGLRENPIRAESLGLDIRRITLLAFAIGSAAGGLAG 232

Query: 328 TLFAARQGFVSPESFTFAESAFVLAIVVLGGMGSQFAVILAAILLVVSRELMRDFNEYSM 387
           +L +    ++ P SF  + S  +L +VV+GG G  F  +L A ++++  E +R    Y +
Sbjct: 233 SLVSPVVQYIEPNSFALSFSLKILLMVVVGGSGYFFGPMLGAAVVILLPEFLRFTEGYYL 292

Query: 388 LMLGGLMVLMMIWRPQGLL 406
           ++   L++L+M++ P GL+
Sbjct: 293 IIYSALVILLMVFSPSGLM 311


Lambda     K      H
   0.330    0.145    0.436 

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: 293
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: 425
Length of database: 337
Length adjustment: 30
Effective length of query: 395
Effective length of database: 307
Effective search space:   121265
Effective search space used:   121265
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: 50 (23.9 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