GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsA in Polaromonas naphthalenivorans CJ2

Align Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate WP_011803051.1 PNAP_RS18440 ABC transporter substrate-binding protein

Query= uniprot:A0A165KPY4
         (416 letters)



>NCBI__GCF_000015505.1:WP_011803051.1
          Length = 416

 Score =  682 bits (1760), Expect = 0.0
 Identities = 330/416 (79%), Positives = 366/416 (87%)

Query: 1   MWKMTKIAAVAVGLAAAMSASAGEVEVLHYWTSGGEAKSVAELKKIMQGKGHTWRDFAVA 60
           M K++K+AA    +AA  +A AGEVEVLHYWTSGGEAKSVAELKKIM+ KGH W+DFAVA
Sbjct: 1   MLKLSKLAAALALVAAGTAAMAGEVEVLHYWTSGGEAKSVAELKKIMEAKGHVWKDFAVA 60

Query: 61  GGGGDSAMTVLKSRVISGNPPSAAQTKGPAIQEWASEGVLANMDTLAKAEKWDELLPKVV 120
           GGGGD+A TVLKSRV+SGNPP+AAQ KGPAIQEWA+EGVLANMD +A+AEKWD LLPKVV
Sbjct: 61  GGGGDNAATVLKSRVVSGNPPAAAQIKGPAIQEWAAEGVLANMDPVAQAEKWDSLLPKVV 120

Query: 121 ADVMKYKGAYVAAPVNVHRVNWMWGSSEALKKAGVAAMPKTWDEFFAAADKLKAAGLVPV 180
           ADVMKYKG +VA PVNVHRVNWMW ++  LKKAGVA MPK WDEFF AADK+K AGL+PV
Sbjct: 121 ADVMKYKGNFVAVPVNVHRVNWMWANAAVLKKAGVAGMPKNWDEFFVAADKIKKAGLIPV 180

Query: 181 AHGGQNWQDFTTFESVVLGVGGAKFYQDALVKLDNTALTSDTMKKSLETFRRIKGYTDPG 240
           AHGGQNWQDFTTFESVVLGVGG KFY DALVKLD  ALT +TMKKSLETFR+IKGYTD  
Sbjct: 181 AHGGQNWQDFTTFESVVLGVGGPKFYSDALVKLDQKALTGETMKKSLETFRKIKGYTDAA 240

Query: 241 APGRDWNLATAMLIQGKAGFQLMGDWAKGEFLAAGKAPGKDFLCAAAPGSANAFTFNVDS 300
           APGRDWNLATAM++Q KA FQ MGDWAKGEF+AAGK PGKDFLCAAAPG+ANAFTFNVDS
Sbjct: 241 APGRDWNLATAMVMQEKAAFQFMGDWAKGEFIAAGKVPGKDFLCAAAPGTANAFTFNVDS 300

Query: 301 FILFKLKDAAAQKAQSDLASSIMSPAFQEVFNLNKGSIPVRAGQPMDKFDDCAKASAKDF 360
           F +FKLK AAAQKAQ+DL+++IM   FQE+FNLNKGSIPVR    M KFDDCAK S KDF
Sbjct: 301 FAMFKLKGAAAQKAQADLSAAIMGTEFQEIFNLNKGSIPVRLNMNMAKFDDCAKLSGKDF 360

Query: 361 VDTAKSGGLVPSAAHGMAIAPATEGAIKDVVSQFWNDDKVSVADAMKKIAAAAKTK 416
           V+TAK+GGLVPSAAHGMAI+PA EGAIKD VSQFWNDDK+SV +A K+IAAAAKTK
Sbjct: 361 VETAKTGGLVPSAAHGMAISPAAEGAIKDAVSQFWNDDKISVDEAQKRIAAAAKTK 416


Lambda     K      H
   0.315    0.128    0.383 

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: 786
Number of extensions: 30
Number of successful extensions: 1
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: 416
Length of database: 416
Length adjustment: 31
Effective length of query: 385
Effective length of database: 385
Effective search space:   148225
Effective search space used:   148225
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: 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