GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Pseudomonas simiae WCS417

Align ornithine aminotransferase (EC 2.6.1.13) (characterized)
to candidate GFF1577 PS417_08025 acetylornithine aminotransferase

Query= BRENDA::B1A0U3
         (469 letters)



>FitnessBrowser__WCS417:GFF1577
          Length = 389

 Score =  266 bits (679), Expect = 1e-75
 Identities = 157/390 (40%), Positives = 221/390 (56%), Gaps = 12/390 (3%)

Query: 48  YHPLPIVFAHAKGSSVWDPEGNKYIDFLSGYSAVNQGHCHPKILKALHDQADRLTVSSRA 107
           Y PL + F    G+ +WD +G +Y+D ++G +  N GH HP+++ A+ +QA  L  +S  
Sbjct: 10  YQPLALSFTRGLGTRLWDQQGREYLDAVAGVAVTNVGHSHPRLVAAISEQAGLLLHTSNL 69

Query: 108 FYNDRFPVFAEYLTALFGYDMVLPMNTGAEGVETALKLARKWGYEKKKIPNDEALIVSCC 167
           +  D     A+ LT L G D     N+GAE  ETALKLAR  G++K     +  L+V   
Sbjct: 70  YSIDWQQRLAQRLTQLSGLDRAFFNNSGAEANETALKLARLHGWKKGI---EAPLVVVME 126

Query: 168 GCFNGRTLGVISMSCDNEATRGFGPLMPGHLKVDFGDAEAIERIFKEKGDRVAAFILEPI 227
             F+GRTLG ++ S       GF  L    LKV FGD  A+E I K  G R+ A +LEPI
Sbjct: 127 NAFHGRTLGTLAASDGPSVRLGFQQLPGDFLKVRFGDLAALEAITKAFGPRITAVLLEPI 186

Query: 228 QGEAGVVIPPDGYLKAVRDLCSKYNVLMIADEIQTGLARTGKMLACDWEDVRPDVVILGK 287
           QGE+GV+  P GYL+A+RD C++   LM+ DEIQTG+ RTG   A   E + PDV+ L K
Sbjct: 187 QGESGVLPAPSGYLQALRDHCTRQGWLMMLDEIQTGIGRTGTWFAFQHEGIVPDVMTLAK 246

Query: 288 ALGGGILPVSAVLADKDVMLCIKPGQHGSTFGGNPLASAVAIAALEVIKEERLTERSTKL 347
            LG G+ P+ A LA   V     PG HGSTFGGNPLA  V    L++I+E+ L + + + 
Sbjct: 247 GLGNGV-PIGACLARAAVAQLFTPGSHGSTFGGNPLACRVGCTVLDIIEEQGLLQNAAQQ 305

Query: 348 GGELLGLLHKIQKKHPEHVKEVRGKGLFIGVELNSESLSPVSGFELSEK-LKERGVLAKS 406
           G  LL  L     +H + V  +RG+GL IG+EL S         +L+++  +E G+L   
Sbjct: 306 GERLLARLRVELNEHAQ-VVAIRGQGLMIGIELASPCR------DLAQRAAQEHGLLINV 358

Query: 407 THDTIIRFTPPLCISADEIQQGSKALAEVL 436
           T   IIR  PPL +   E++   +A+  +L
Sbjct: 359 TRGKIIRLLPPLTLDTQEVEMIVRAITRLL 388


Lambda     K      H
   0.319    0.137    0.409 

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: 409
Number of extensions: 20
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: 469
Length of database: 389
Length adjustment: 32
Effective length of query: 437
Effective length of database: 357
Effective search space:   156009
Effective search space used:   156009
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:

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