GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Rhodospirillum rubrum ATCC 11170

Align Leucine ABC transporter subunit substrate-binding protein LivK (characterized, see rationale)
to candidate YP_426833.1 Rru_A1746 extracellular ligand-binding receptor

Query= uniprot:A0A160A0J6
         (375 letters)



>NCBI__GCF_000013085.1:YP_426833.1
          Length = 368

 Score =  296 bits (759), Expect = 5e-85
 Identities = 148/356 (41%), Positives = 222/356 (62%), Gaps = 2/356 (0%)

Query: 11  LFAAMVLAGVASHSFAADTIKIGIAGPKTGPVAQYGDMQFSGSKMAIEQINAKGGVNGKQ 70
           L AA     +   S  AD I +G+AGP TG  A +G+    G++ A++ INAKGGV G++
Sbjct: 8   LLAATAAFAMGVGSAQAD-ITVGVAGPMTGQYASFGEQLAKGAEQAVKDINAKGGVLGEK 66

Query: 71  LVAVEYDDACDPKQAVAVANKVVNDGIKFVVGHLCSSSTQPASDIYEDEGVVMITPAATS 130
           LV  + DDACDPKQAVAVAN+ VND + FV GH CS S+ PAS +Y +EG+V I+PA+T+
Sbjct: 67  LVLKKGDDACDPKQAVAVANQFVNDKVVFVAGHFCSGSSIPASAVYNEEGIVQISPASTN 126

Query: 131 PDITARGYKMIFRTIGLDSAQGPAAGNYIADHVKPKIVAVLHDKQQYGEGIASAVKKTLE 190
           P +T +G++ +FRT G D  QGP AG+++  H   + +A++HDK  YG+G+A   K  L 
Sbjct: 127 PKLTEQGFENVFRTCGRDDQQGPTAGDFLKAHFPGQKIAIIHDKTAYGKGLADETKSALN 186

Query: 191 DKGVKVAVFEGVNAGDKDFSSMIAKLKQANVDFVYYGGYHPELGLILRQSQEKGLKAKFM 250
             GV+ A++E + AG+KD+S+++ KLK   +  +Y GGYH E GLI+RQ++E+GL A+ +
Sbjct: 187 KAGVQEALYEAITAGEKDYSALVTKLKNEGIKIIYLGGYHTEAGLIIRQAKEQGLDARIV 246

Query: 251 GPEGVGNDSISQIAKESSEGLLVTLPKSFDQDPANIALADAFKAKKEDPSGPFVFPSYSA 310
             + + +   + IA  + +G L T      ++P   A+  +F     +  G +   +Y A
Sbjct: 247 SGDALVSSEFASIAGPAGDGTLFTFSPDPRKNPEAAAVVKSFTDAGYNAEG-YTLYTYGA 305

Query: 311 VTVIADAIKAAKSEDAGKVAEAIHAGTFKTPTGDLSFDKNGDLKDFKFVVYEWHFG 366
           V   A A++ AKS D  KVA+A+ +G F T  G + FD  GD+    +V+YEW  G
Sbjct: 306 VQAWAQAVEKAKSTDVDKVAKALKSGQFSTVLGPIGFDAQGDVSAPGYVMYEWKGG 361


Lambda     K      H
   0.314    0.132    0.372 

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: 460
Number of extensions: 27
Number of successful extensions: 2
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: 375
Length of database: 368
Length adjustment: 30
Effective length of query: 345
Effective length of database: 338
Effective search space:   116610
Effective search space used:   116610
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 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