GapMind for catabolism of small carbon sources

 

Aligments for a candidate for rocD in Pseudomonas fluorescens GW456-L13

Align ornithine δ-aminotransferase (EC 2.6.1.13) (characterized)
to candidate PfGW456L13_1158 Acetylornithine aminotransferase (EC 2.6.1.11)

Query= metacyc::MONOMER-16810
         (468 letters)



>lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1158
           Acetylornithine aminotransferase (EC 2.6.1.11)
          Length = 427

 Score =  212 bits (539), Expect = 2e-59
 Identities = 139/391 (35%), Positives = 200/391 (51%), Gaps = 15/391 (3%)

Query: 39  IEYESDYSAHNYHPIPMVFSKAKDVHVWDPEGRKYLDFLSAYSAVNQGHCHEKILNALSQ 98
           +   S+Y   +      VF + +   +WD + R YLDF     A + GH    ++NA++ 
Sbjct: 27  VNLSSEYLMPSVERPKQVFVRGQGSWLWDSDDRAYLDFSQGGGANSLGHSPSVLVNAITA 86

Query: 99  QAQQLTLSSRAFHNDIFPIFAQHLTSMFGYEMILPMNTGAEGVETALKLARKWGYEKKHI 158
           QAQ L       HN      A+HL +  G +    +NTG+E  E A+KLARKWG  ++H 
Sbjct: 87  QAQSLINPGFGLHNRGMLSLAEHLCASTGSDQAYLLNTGSEACEAAIKLARKWG--QRHR 144

Query: 159 PKNEAIIISCCGCFHGRTTAVISMSCDNEATRGFGPFLPGLLKVDFGDADSLKSMFEAHG 218
                II++  GC HGR+ A IS S  +     F P LPG  +V F D   L ++  A  
Sbjct: 145 GGASRIIVANNGC-HGRSLATISASDSSTLANRFEPQLPGFSRVPFND---LPALHAAVD 200

Query: 219 DKVAGFLFEPIQGEAGVIVPPKGYLQSVRELCSKYNVLMIADEIQTGIGRTGKLLACEWE 278
           ++    + EPIQ EAGV+     YL+ V  LC +  +L+I DE+QTGIGR G LLA +  
Sbjct: 201 ERTVAIMLEPIQSEAGVVPATVHYLKGVERLCRELGILLIFDEVQTGIGRCGSLLAEQSC 260

Query: 279 SVRPDVVILGKALGGGVLPVSAVLADKDIMLCFKPGEHGSTFGGNPLASAVAIAALEIVE 338
            V  D+V+LGK LGGGV P++A+LA +    CF  GE   T  GN L +A  ++ L+ V+
Sbjct: 261 GVTADIVVLGKGLGGGV-PLAALLA-RGKACCFDIGELAGTHHGNALMTAAGLSVLDTVQ 318

Query: 339 EEKLAERAAEMGQVFRSQFLDIQKAYPHIIKEVRGQGLLNAVELNAKGLSTVSAFDICQR 398
           ++   +  AE GQ  R     +   Y H   E+RGQGLL  +      LS  SA  + + 
Sbjct: 319 DKAFLKHVAEAGQHLREGLGRLAHRYGH--GELRGQGLLWGLT-----LSDDSADAVVKA 371

Query: 399 LKERGVLAKPTHGTIIRFSPPLTIRLKELTE 429
               G+L        +RF+P L +    + E
Sbjct: 372 ALYEGLLLNAPQADCLRFTPALNVSNANIDE 402


Lambda     K      H
   0.319    0.136    0.405 

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: 460
Number of extensions: 23
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: 468
Length of database: 427
Length adjustment: 33
Effective length of query: 435
Effective length of database: 394
Effective search space:   171390
Effective search space used:   171390
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 (21.8 bits)
S2: 51 (24.3 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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