GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Rhizobium johnstonii 3841

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate WP_003542332.1 RL_RS19315 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>NCBI__GCF_000009265.1:WP_003542332.1
          Length = 373

 Score =  410 bits (1054), Expect = e-119
 Identities = 204/360 (56%), Positives = 258/360 (71%), Gaps = 3/360 (0%)

Query: 4   KLSLLVAVAATAMTA--SVAKADIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGV 61
           K SLL AVA TAM A    A AD+ +A AGP+TG  A FG Q++KG EQA ADINAAGG+
Sbjct: 2   KKSLLSAVALTAMVAFSGNAWADVLIAVAGPLTGPNAAFGAQLQKGAEQAAADINAAGGI 61

Query: 62  LGQKLKLEVGDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISP 121
            G+++K+E+GDD  DPKQ ++VAN+ A  GVKFV GHF SG SIPAS+VYAE G+L+I+P
Sbjct: 62  NGEQIKIELGDDVSDPKQGISVANKFAADGVKFVIGHFNSGVSIPASEVYAENGILEITP 121

Query: 122 ASTNPKLTEQNLKNVFRVCGRDDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQ 181
           A+TNP  TE+ L N FR CGRDDQQG IAGKYL +++K   +A++HDK+ YG+GLADET+
Sbjct: 122 AATNPTFTERGLWNTFRTCGRDDQQGAIAGKYLADHFKDAKIAVVHDKTPYGQGLADETK 181

Query: 182 KALNAGGQKEKIYEAYTAGEKDYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLN 241
           KA+NA G  E IYE    G+KD+SAL++K+K+  V ++Y GG HTEAGL+ RQ  DQGL 
Sbjct: 182 KAMNAAGVTEVIYEGINVGDKDFSALIAKMKEAGVSIIYWGGLHTEAGLIIRQAADQGLK 241

Query: 242 APIVSGDALVTNEYWAITGPAGENTMMTFGPDPREMPEAKEAVEKFRKAGYEPEGYTLYT 301
           A +VSGD +V+NE  +I G A   T+ TFGPDP   P  KE VEKF+ AG+ PE YTLY+
Sbjct: 242 ATLVSGDGIVSNELASIAGDAVAGTLNTFGPDPTANPANKELVEKFKAAGFNPEAYTLYS 301

Query: 302 YAALQIWAEAAKQANSTDSAKIADVLR-KNSYNTVIGKIGFDAKGDVTSPAYVWYRWNNG 360
           YAA+Q  A AAK A S D   +A  ++ K  + TV+G I FD KGD   P Y+ Y W  G
Sbjct: 302 YAAMQTIAGAAKAAGSLDPEAVAKAMKEKGPFPTVLGDISFDEKGDPKIPGYIMYEWKKG 361


Lambda     K      H
   0.312    0.129    0.366 

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: 481
Number of extensions: 18
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: 366
Length of database: 373
Length adjustment: 30
Effective length of query: 336
Effective length of database: 343
Effective search space:   115248
Effective search space used:   115248
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 (21.9 bits)
S2: 49 (23.5 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