GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Pseudomonas fluorescens FW300-N2E2

Align Ornithine aminotransferase; OAT; EC 2.6.1.13; Ornithine--oxo-acid aminotransferase (uncharacterized)
to candidate Pf6N2E2_5326 Acetylornithine aminotransferase (EC 2.6.1.11)

Query= curated2:Q89RB7
         (404 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5326
          Length = 396

 Score =  268 bits (684), Expect = 3e-76
 Identities = 159/388 (40%), Positives = 221/388 (56%), Gaps = 13/388 (3%)

Query: 20  YEPIGVVLSRGEGVWVWDTDGNRYLDCLSAYSAVSQGHCHPKILAAMVEQAHRLTLTSRA 79
           Y+P+ +  + G G  +WD DG  YLD ++  +  + GH HP+++AA+ EQA  L  TS  
Sbjct: 15  YQPLALSFTHGLGTRLWDQDGREYLDAVAGVAVTNVGHSHPRLVAAISEQAGLLLHTSNL 74

Query: 80  FHNDQLAPFYEEIAALTGSHKVLPMNSGAEAVESAIKSVRKWGYEVKGVPDDQAEIIVCA 139
           +  D      +++  L+G  +    NSGAEA E+A+K  R +G+  KG+  +Q  ++V  
Sbjct: 75  YSIDWQQRLAQKLTQLSGLERAFFNNSGAEANETALKLARLYGWH-KGI--EQPLVVVMD 131

Query: 140 DNFHGRTLGIVGFSTDPETRGHFGPFAPGFRIIPFGDAAALE---QAITPNTVAFLVEPI 196
           + FHGRTLG +  S  P  R  F      F  +PFGD AALE   QA     VA LVEPI
Sbjct: 132 NAFHGRTLGTMCASDGPSVRLGFNRLPGDFIKVPFGDLAALEAIQQAHAERIVAVLVEPI 191

Query: 197 QGEAGVIIPPAGYFTKVRELCTANNVMLVLDEIQTGLGRTGKLLAEQHEGIEADVTLLGK 256
           QGE+GV + P GY   +RELC+    +L+LDEIQTG+GRTG+  A QHEGI  DV  L K
Sbjct: 192 QGESGVQLAPPGYLKALRELCSRRAWLLMLDEIQTGIGRTGQWFAFQHEGIVPDVMTLAK 251

Query: 257 ALAGGFYPVSAVLSNNEVLGTLRPGQHGSTFGGNPLACAVARAAMRVLVEEGMIENAARQ 316
            L  G  P+ A L+  +      PG HGSTFGGNPLAC V    + ++ ++ +++NA  Q
Sbjct: 252 GLGNG-VPIGACLARGKAAELFTPGSHGSTFGGNPLACRVGCTVLEIIEQQALVDNARHQ 310

Query: 317 GARLLEGLKDIRAN--TVREVRGRGLMLAVEL-HPEAGRARRYCEALQGKGILAKDTHGH 373
           G +LL  L+   A+   V  +RG+GLM+ +EL  P    A R   A +  G+L   T G 
Sbjct: 311 GDQLLGRLRIELADNPNVLAIRGQGLMIGIELKQPVRDLALR---AARDHGLLINITRGQ 367

Query: 374 TIRIAPPLVITSDEVDWALEQFATTLTQ 401
           TIR+ PPL I   EV+  +   +  L Q
Sbjct: 368 TIRLLPPLTIDGREVEMIVRGVSRCLAQ 395


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: 467
Number of extensions: 21
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: 404
Length of database: 396
Length adjustment: 31
Effective length of query: 373
Effective length of database: 365
Effective search space:   136145
Effective search space used:   136145
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: 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