GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ1 in Cupriavidus basilensis 4G11

Align Beta-ketoadipyl CoA thiolase (EC 2.3.1.-) (characterized)
to candidate RR42_RS07610 RR42_RS07610 acetyl-CoA acetyltransferase

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



>FitnessBrowser__Cup4G11:RR42_RS07610
          Length = 393

 Score =  316 bits (809), Expect = 9e-91
 Identities = 186/409 (45%), Positives = 259/409 (63%), Gaps = 22/409 (5%)

Query: 7   LKDAYIVDAIRTPIGRYGGALSAVRADDLGAIPIKALAERYPDLDWSKIDDVLYGCANQA 66
           + D  IV A RT +G++GG+L+ + A +LGAI IKA  ER   +   ++ +V+ G    A
Sbjct: 1   MTDIVIVSAARTAVGKFGGSLAKIPAPELGAIVIKAALER-AGVKPEQVSEVIMGQVLTA 59

Query: 67  GEDNRDVARMSLLLAGLPVDVPGSTINRLCGSGMDAVGSAARAIRTGETQLMIAGGVESM 126
           G   ++ AR + L AGLPV VP  TIN++CGSG+ AV  AA AI  G+ ++++AGG E+M
Sbjct: 60  GS-GQNPARQAALKAGLPVMVPAMTINKVCGSGLKAVMLAANAIAAGDAEIVVAGGQENM 118

Query: 127 SRAPFVM-GKADSAFSRKAEIFDTTIG---WRFVNPVLKKQYGIDSMPETAENVAADFGI 182
           S AP V+ G  D      A++ D+ I    W   N     QY    M  TAENVA ++GI
Sbjct: 119 SAAPHVLPGSRDGFRMGDAKLIDSMIVDGLWDVYN-----QY---HMGVTAENVAKEYGI 170

Query: 183 SREDQDAFALRSQQRTAAAQKEGRLAAEITPVTIPRRKQDPLVVDTDEHPRE-TSLEKLA 241
           +RE QDAFA  SQ +  AAQK G+   EI PV IP+RK DP++  TDE  R   + + LA
Sbjct: 171 TREAQDAFAAGSQNKAEAAQKAGKFDEEIVPVPIPQRKGDPVMFATDEFVRHGVTQDALA 230

Query: 242 SLPTPFRENGTVTAGNASGVNDGACALLLAGADALKQYNLKPRARVVAMATAGVEPRIMG 301
            L   F + G+VTA NASG+NDGA A+++  A   K+  L P A + A  TAGV+P++MG
Sbjct: 231 GLKPAFDKAGSVTAANASGLNDGAAAVVVMSAAKAKELGLTPLATIRAYGTAGVDPKVMG 290

Query: 302 FGPAPATRKVLATAGLELADMDVIELNEAFAAQALAVTRDLGLPDDAEHVNPNGGAIALG 361
            GP PA+++ L+ AG  + ++D++E+NEAFAAQALAV + +G   D   VN NGGAIA+G
Sbjct: 291 MGPVPASKRCLSRAGWSVEELDLMEINEAFAAQALAVHKQMGW--DTSKVNVNGGAIAIG 348

Query: 362 HPLGMSGARLVTTALNELERRHAAGQKARYALCTMCIGVGQGIALIIER 410
           HP+G SG R++ T L+E++RR      A   L ++CIG G G+AL +ER
Sbjct: 349 HPIGASGCRILVTLLHEMKRR-----DAHKGLASLCIGGGMGVALAVER 392


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: 427
Number of extensions: 20
Number of successful extensions: 6
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 Sep 17 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