GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Klebsiella variicola At-22

Align muconate cycloisomerase (EC 5.5.1.1) (characterized)
to candidate WP_181403700.1 KVAR_RS12085 muconate cycloisomerase family protein

Query= metacyc::MONOMER-14643
         (382 letters)



>NCBI__GCF_000025465.1:WP_181403700.1
          Length = 387

 Score =  417 bits (1072), Expect = e-121
 Identities = 213/371 (57%), Positives = 272/371 (73%), Gaps = 1/371 (0%)

Query: 2   LATAIESIETIIVDLPTIRPHKLAMHTMQNQTLVIIRVRCADGIEGIGESTTIGGLAYGN 61
           +   +E IE+ IVD+PTIRPHKL+M TM  QTLVI+R+  +DGI GIGE+TTIGGL+YG 
Sbjct: 16  MTATVERIESWIVDVPTIRPHKLSMTTMGCQTLVIVRLTRSDGICGIGEATTIGGLSYGV 75

Query: 62  ESPDSIKTNIDKHFAPLLIGQDSGNVNAAMLRLERSIRGNTFAKSGIETALLDAHGKRLG 121
           ESP++I + I  +  PLL G  + N+NA   R+  +IRGNTFAKS IETALLDA GK LG
Sbjct: 76  ESPEAISSAITHYLTPLLKGLPADNLNALTARMNSAIRGNTFAKSAIETALLDAQGKALG 135

Query: 122 LPVSELLGGRVRDALPVAWTLASGDTEKDIAEAEKMLDLRRHRIFKLKIGAGEVNRDLAH 181
           LPVS LLGG ++ +LPV WTLASGDT KDIAE EK+L  RRH+ FKLKIGA E+  DL H
Sbjct: 136 LPVSALLGGALQTSLPVLWTLASGDTAKDIAEGEKLLAERRHQAFKLKIGARELATDLRH 195

Query: 182 VIAIKKALGDRASVRVDVNQAWDEAVALRACRILGTNGIDLVEQPISRNNRGGMARLNAM 241
             AI +ALGDRAS+RVDVNQAWD A   + CR L   G+DL+EQP+S ++   + RL+  
Sbjct: 196 TRAIVEALGDRASIRVDVNQAWDAATGAKGCRELAAMGVDLIEQPVSAHDNAALVRLSQH 255

Query: 242 SPAPIMADESIECVEDAFNLAREGAASVFALKIAKNGGPRAVLRTASIAEAAGIALYGGT 301
               I+ADE++    D + LA++G    +ALKIAK GGP +VL  A +A+AAG+ LYGGT
Sbjct: 256 IETAILADEAVATAYDGYQLAQQGFTGAYALKIAKAGGPNSVLALARVAQAAGVGLYGGT 315

Query: 302 MLEGGLGTMASAHAFVTLNKLAWDTELFGPLLLTEDILSEPLVYRDFELHVPNTPGLGLS 361
           MLEG +GT+AS HA+ TL  L W TE+FGPLLL +DI+S PL + D ++ +P TPGLG+ 
Sbjct: 316 MLEGTVGTVASLHAWSTL-PLQWGTEMFGPLLLKDDIVSVPLTFADGQVALPQTPGLGVE 374

Query: 362 LDEERLAFFRR 372
           LDE++L F+ R
Sbjct: 375 LDEDKLRFYSR 385


Lambda     K      H
   0.319    0.136    0.386 

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: 354
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: 382
Length of database: 387
Length adjustment: 30
Effective length of query: 352
Effective length of database: 357
Effective search space:   125664
Effective search space used:   125664
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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