GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Pseudomonas simiae WCS417

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate GFF3717 PS417_19025 aspartate aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__WCS417:GFF3717
          Length = 401

 Score =  195 bits (495), Expect = 2e-54
 Identities = 127/366 (34%), Positives = 189/366 (51%), Gaps = 15/366 (4%)

Query: 30  QGEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQA 89
           QG +I+  +VG+PDFDTPA I+ AA  ++  G+THY    G  ALRQ I  + ++ +  A
Sbjct: 30  QGRDIVNFTVGEPDFDTPAHILAAASQAMHNGDTHYTSTTGTLALRQAICLKLQQDNDLA 89

Query: 90  VDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSEN 149
              ++VV   G +  +Y  +   LN GDEVIV  P +V+Y  +     A  V +P     
Sbjct: 90  YGLDEVVAGCGGKHVIYHALAATLNRGDEVIVHTPYWVSYPDIARLNDATPVIIPGDESL 149

Query: 150 GFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWMISDEVYS 208
           GF++  + +   IT RT+ + LNSP+NPSGA        ALA++   H  + +++DE+Y 
Sbjct: 150 GFKLSPDALEQAITARTKWVILNSPNNPSGAVYNETELLALAQVLRRHPHVLIMADEIYE 209

Query: 209 ELLFD-GEHVSPASL-PGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCM 266
             ++    HV    L P +  RT  +N  SK +AMTGWR+G+  GPA L A +  L    
Sbjct: 210 HFIYGRARHVPLTRLAPDLKPRTLIVNGASKGYAMTGWRLGFGAGPAWLIAAIAKLLSQT 269

Query: 267 LYGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMV 326
                   Q AA  A       + AMRE Y++RR  ++  LAD PGL    PDG  +V  
Sbjct: 270 TTCPSSLSQAAAVAAFTGDQAPIAAMREEYQQRRARMLALLADIPGLSCTPPDGAFYVFA 329

Query: 327 DI-------RPTG---LSAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVLGAEPLR 376
           ++        P G    S     D LL  +G++ ++G A+G S   ++RL     +E + 
Sbjct: 330 NVSGLMGKLTPQGDRLDSDTQLVDYLLRDYGLATVSGAAYGMSP--YVRLSFASSSEVIE 387

Query: 377 EACRRI 382
           E CRR+
Sbjct: 388 EGCRRL 393


Lambda     K      H
   0.322    0.136    0.411 

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: 414
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: 393
Length of database: 401
Length adjustment: 31
Effective length of query: 362
Effective length of database: 370
Effective search space:   133940
Effective search space used:   133940
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 (21.9 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