GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Dyella japonica UNC79MFTsu3.2

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate N515DRAFT_2688 N515DRAFT_2688 acetyl-CoA acyltransferase

Query= metacyc::MONOMER-20679
         (395 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2688
          Length = 401

 Score =  281 bits (718), Expect = 3e-80
 Identities = 171/397 (43%), Positives = 230/397 (57%), Gaps = 11/397 (2%)

Query: 3   EAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRA-GIDPKEVEDVVMGAAMQQG 61
           +A IV+  RTP+GKA RG    T    +L H I   + +A GID   + DV++G AM + 
Sbjct: 7   DAYIVAATRTPVGKAPRGVFRNTRPDDMLAHVIRAVMAQAPGIDAHRIGDVIVGCAMPEA 66

Query: 62  ATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESIS 121
             G N+AR  LL AGLP T  G T++R C+SG+QAIA AA  +     ++ +  G ES+S
Sbjct: 67  EQGMNVARIGLLLAGLPDTVPGVTVNRFCSSGVQAIAQAADRIRLGEADLMIAAGTESMS 126

Query: 122 LVQNDKMNTFHAVDPAL---EAIKGDVYMAMLDTAETVAKRYGISRERQDEYSLESQRRT 178
           +V    M    A++P +   E I   +   M  TAE VAK++ ISRE QD ++  S  R 
Sbjct: 127 MVP--MMGHKVAMNPGIFDNEHI--GIAYGMGITAENVAKQWKISREEQDTFAAASHERA 182

Query: 179 AAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLKAV-- 236
            AA + G+F DEI P        D AT ++      +  DEGPRP +T E L  LK V  
Sbjct: 183 LAAIKAGEFKDEITPFKLDDHYPDLATRSIKTDSRLIDTDEGPRPGSTVEVLGKLKPVFR 242

Query: 237 RGE-GFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPDEMGIGPV 295
            G+ G ++TAGN+SQ SDGA A ++ S+      GL P+  F      G  PD MGIGP 
Sbjct: 243 NGQFGGSVTAGNSSQTSDGAGAVLLASEAAIKEYGLTPIARFVSYSVAGVRPDIMGIGPK 302

Query: 296 FAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISVGHPYGMS 355
            A+P+ LK+ G++ D +   ELNEAFA Q L     LG+DP K+N  GGAI++GHP G +
Sbjct: 303 EAIPKALKQAGMTQDQLDWIELNEAFAAQSLAVIKDLGLDPSKINPLGGAIALGHPLGAT 362

Query: 356 GARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFE 392
           GA  A   +   RRRK KY +VTMC+G GMG+AG+FE
Sbjct: 363 GAIRAATLVHGMRRRKQKYGMVTMCIGTGMGAAGIFE 399


Lambda     K      H
   0.316    0.134    0.378 

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: 417
Number of extensions: 16
Number of successful extensions: 4
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: 395
Length of database: 401
Length adjustment: 31
Effective length of query: 364
Effective length of database: 370
Effective search space:   134680
Effective search space used:   134680
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 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