GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aapJ in Marinomonas arctica 328

Align AapJ, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized)
to candidate WP_111605657.1 DK187_RS01945 amino acid ABC transporter substrate-binding protein

Query= TCDB::Q52812
         (341 letters)



>NCBI__GCF_003259225.1:WP_111605657.1
          Length = 343

 Score =  316 bits (810), Expect = 5e-91
 Identities = 162/345 (46%), Positives = 222/345 (64%), Gaps = 6/345 (1%)

Query: 1   MKNKLLSAAIGAAVLAVGASA-ASATTLSDVKAKGFVQCGVNTGLTGFAAPDASGNWAGF 59
           MK   L+ A    +LA  + A  SA+TLS VK +G+V C +     GF + + +G W G 
Sbjct: 1   MKKFSLALAATTTLLAANSYADESASTLSAVKDRGYVNCVIGNSFPGFYSLNKAGEWQGM 60

Query: 60  DVDFCKAVASAVFGDPTKVKYTPTNAKERFTALQSGEIDVLSRNTTWTINRDTALGFNFR 119
           D+D C+ VASAVFGD +KV + P    + FT+++SG+ D+LS+  TWT++RDT  G +F 
Sbjct: 61  DIDMCRGVASAVFGDASKVTFLPVQWAQSFTSIKSGQGDILSKGMTWTLSRDTQQGLDFL 120

Query: 120 PVTYYDGQGFMVRKGLNVKSALELSGAAICVQSGTTTELNLADYFKTNNLQYNPVVFENL 179
              +YDGQGFMVRK L VKS  EL GA +CV +GT++ELN+ADY + N+L    VVF++ 
Sbjct: 121 DTYFYDGQGFMVRKDLGVKSVKELKGATVCVLTGTSSELNIADYSRANDLDIKTVVFDDS 180

Query: 180 PEVNAAYDAGRCDVYTTDQSGLYSLRLTLKNPDEHIILPEIISKEPLGPAVRQGDDQWFD 239
              N A+    CD  T D+SGL + R    NP +++ILPE ISKE L  AV+Q D +W +
Sbjct: 181 SVRNTAFFNNNCDALTNDKSGLAAQRSAAPNPSDYVILPETISKEALSFAVKQNDSEWAN 240

Query: 240 IVSWTAYALINAEEFGITQANVDEMK-NSPNPDIKRFLGSETDTKIGTDLGLTNDWAANV 298
           +V WT  A++ AEEFG+   NV++M+ +S +P ++R LG E D  +G  LGL  DWA  V
Sbjct: 241 VVKWTFAAMVAAEEFGVNSQNVEQMRADSQSPVVRRLLGVEGDLHVG--LGLPQDWAYQV 298

Query: 299 IKGVGNYGEIFERNIGQGSPLKIARG--LNALWNKGGIQYAPPVR 341
           IK VGNYGE++ERN+G  S L + R   LNALW  GG+ YA   R
Sbjct: 299 IKNVGNYGEVYERNVGVNSVLGLDRDGTLNALWTDGGMMYAKSFR 343


Lambda     K      H
   0.316    0.134    0.398 

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: 356
Number of extensions: 22
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: 341
Length of database: 343
Length adjustment: 29
Effective length of query: 312
Effective length of database: 314
Effective search space:    97968
Effective search space used:    97968
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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