GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Sphingomonas koreensis DSMZ 15582

Align Ornithine aminotransferase 1; OAT 1; EC 2.6.1.13; Ornithine--oxo-acid aminotransferase 1 (uncharacterized)
to candidate Ga0059261_3205 Ga0059261_3205 transaminase, acetylornithine/succinylornithine family

Query= curated2:Q4A0N2
         (394 letters)



>FitnessBrowser__Korea:Ga0059261_3205
          Length = 398

 Score =  229 bits (583), Expect = 1e-64
 Identities = 134/380 (35%), Positives = 205/380 (53%), Gaps = 9/380 (2%)

Query: 16  YSPLKLALAKGRGAKVWDIEDNCYIDCISGFSVVNQGHCHPKIIKALQEQSQRITMVSRA 75
           Y   ++   +G G  +       Y+D  +G +V   GH HP+  KA+ EQ+  +  VS  
Sbjct: 10  YPRCEVRPVRGEGCYLIGERGERYLDFAAGIAVNALGHGHPQFTKAIAEQAATLMHVSNL 69

Query: 76  LYSDNLGKWEEKICKLANKENVLPMNTGTEAVETAIKMARKWGADIKNIDESSSEIIAMN 135
             S       ++I   +  + V   N+G EA+E AIK AR++     N +    ++I   
Sbjct: 70  YGSPQGEALAQRIVDNSFADTVFFTNSGVEAIECAIKTARRY--HYVNGNPQRHKLITFK 127

Query: 136 GNFHGRTLGSLSLSSQDSYKKGFGPLLNNIHYADFGDIEQLKKLINNQTTAIILEPIQGE 195
             FHGR++G++S + Q   + GF PLL    Y  F D+E     I+++T   ++E +QGE
Sbjct: 128 NAFHGRSIGAISATDQPKMRDGFEPLLPGFDYVKFNDLEGAIAKIDDETAGFLVETVQGE 187

Query: 196 GGVNIPPTHFIQEVRQLCNEYNVLLIADEIQVGLGRTGKMFAMEWENTEPDIYLLGKSLG 255
           GG+      FIQ +R+ C+E+ +LLI DEIQ G GRTGKM+A E     PDI    K +G
Sbjct: 188 GGMTAGTVEFIQGLRKACDEHGLLLILDEIQCGYGRTGKMWAYEHYGITPDILTAAKGIG 247

Query: 256 GGLYPISAVLANQDVMSVLTPGTHGSTFGGNPLACAVSMAALDVLNEEHLVQNALDLGDR 315
            G +P+ A LA ++    +T GTHGST+GGNPLA A   A LDV+ E    ++   +G+R
Sbjct: 248 NG-FPLGACLATEEAAKGMTFGTHGSTYGGNPLAMAAGQAVLDVMLEPGFFEHVEKMGER 306

Query: 316 LLKHLQQI---ESELIVEVRGRGLFIGIELN--VAAQDYCEQM-INKGVLCKETQGNIIR 369
           L    +Q+      L  E+RG+GL +GI+L     ++D+   +  N G+L      N+ R
Sbjct: 307 LRAGFEQLIPNHDHLFDEIRGKGLMLGIKLKEPAVSRDFVAHLRENHGLLTVAAGENVFR 366

Query: 370 IAPPLVIDKDEIDEVIRVIT 389
           + PPLVI++  I E I  ++
Sbjct: 367 VLPPLVIEESHIAECIEKLS 386


Lambda     K      H
   0.317    0.136    0.396 

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: 393
Number of extensions: 25
Number of successful extensions: 5
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: 394
Length of database: 398
Length adjustment: 31
Effective length of query: 363
Effective length of database: 367
Effective search space:   133221
Effective search space used:   133221
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