GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Desulfoscipio geothermicus DSM 3669

Align Beta-ketoadipyl CoA thiolase (EC 2.3.1.-) (characterized)
to candidate WP_092487318.1 BM299_RS17115 acetyl-CoA C-acetyltransferase

Query= reanno::Marino:GFF2751
         (415 letters)



>NCBI__GCF_900115975.1:WP_092487318.1
          Length = 393

 Score =  345 bits (885), Expect = 1e-99
 Identities = 194/405 (47%), Positives = 263/405 (64%), Gaps = 15/405 (3%)

Query: 7   LKDAYIVDAIRTPIGRYGGALSAVRADDLGAIPIKALAERYPDLDWSKIDDVLYGCANQA 66
           +KD  IV   RTPIG +GGAL +V A  L  + IK + +R   ++ ++IDDV+ GC  Q+
Sbjct: 1   MKDVVIVAGARTPIGDFGGALRSVTAGQLAVVVIKEVIKR-TGVNPAEIDDVILGCCVQS 59

Query: 67  GEDNRDVARMSLLLAGLPVDVPGSTINRLCGSGMDAVGSAARAIRTGETQLMIAGGVESM 126
            E+  ++ R + L+AGLP +V G TI R C SGM A+ S  + I TG++++++AGG ESM
Sbjct: 60  SEEP-NIGRTAALMAGLPDNVTGMTIQRQCASGMQAIISGYQQIITGDSEIVLAGGTESM 118

Query: 127 SRAPFVMGKADSAFSRKAEIFDTTIGWRFVNPVLKKQYGIDSMPETAENVAADFGISRED 186
           S AP+V+ KA      +   F   +     +P+ K   G     ETAE +A  +GI+RE+
Sbjct: 119 STAPYVLKKARWGMRLQHGEFTDALWETLTDPIHKIMMG-----ETAERLADKYGITREE 173

Query: 187 QDAFALRSQQRTAAAQKEGRLAAEITPVTIPRRKQDPLVVDTDEHPR-ETSLEKLASLPT 245
           QD  A RS Q    A ++G  A EI PV +PRRK D ++VD DEHPR + S+EKLA L  
Sbjct: 174 QDIIAYRSHQNAINAIEKGYFAGEIVPVPVPRRKGDLVLVDRDEHPRNDISMEKLAKLSP 233

Query: 246 PFRENGTVTAGNASGVNDGACALLLAGADALKQYNLKPRARVVAMATAGVEPRIMGFGPA 305
            FR+NGTVTAGNASG+ND A  +LL   +  +Q  LKP AR+V+ A AGVEP +MG+GP 
Sbjct: 234 AFRKNGTVTAGNASGLNDAAAGVLLMSEEKARQLGLKPLARIVSHARAGVEPDLMGYGPV 293

Query: 306 PATRKVLATAGLELADMDVIELNEAFAAQALAVTRDLGLPDDAEHVNPNGGAIALGHPLG 365
           PA +K L  AGL LAD+D+IELNEAFAAQ LA  + L L  + E VN NG  + LGHP+G
Sbjct: 294 PAIKKALQRAGLALADIDLIELNEAFAAQYLACEKLLDL--NREIVNVNGSGVGLGHPVG 351

Query: 366 MSGARLVTTALNELERRHAAGQKARYALCTMCIGVGQGIALIIER 410
            +G R+V T LNE+ERR+     A Y L ++C+G G G+A+I+ER
Sbjct: 352 CTGTRIVVTLLNEMERRN-----AHYGLASLCVGGGMGVAVIVER 391


Lambda     K      H
   0.318    0.133    0.382 

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: 441
Number of extensions: 26
Number of successful extensions: 7
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: 415
Length of database: 393
Length adjustment: 31
Effective length of query: 384
Effective length of database: 362
Effective search space:   139008
Effective search space used:   139008
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 (21.7 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