GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argF' in Pseudomonas fluorescens FW300-N2C3

Align N-acetylornithine carbamoyltransferase (EC 2.1.3.9) (characterized)
to candidate AO356_18275 AO356_18275 ornithine carbamoyltransferase

Query= BRENDA::Q8P8J2
         (339 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_18275
          Length = 306

 Score =  117 bits (292), Expect = 5e-31
 Identities = 101/340 (29%), Positives = 152/340 (44%), Gaps = 47/340 (13%)

Query: 1   MSLKHFLNTQDWSRAELDALLTQAALFK----RNKLGSELKGKSIALVFFNPSMRTRTSF 56
           MS +HFL+  D++  EL  ++ +    K    R  L   LK + + ++F   S RTR SF
Sbjct: 1   MSARHFLSLMDFTPDELLGVIRRGVELKDLRNRGVLFEPLKNRVLGMIFEKSSTRTRISF 60

Query: 57  ELGAFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVLGRYVDLIGVRAFPK 116
           E G  QLGG A+ L P       +  LG        E I + A V+   +D + +R F  
Sbjct: 61  EAGMIQLGGQAIFLSPR------DTQLGR------GEPIGDCAIVMSSMLDAVMIRTFAH 108

Query: 117 FVDWSKDREDQVLKSFAKYSPVPVIN-METITHPCQELAHALALQEHFGTPDLRGKKYVL 175
                       L  FA +S VPVIN +    HPCQ LA      EH G+  ++GK   +
Sbjct: 109 ----------STLTEFAAHSRVPVINGLSDDLHPCQLLADMQTFLEHRGS--IQGK--TV 154

Query: 176 TWTYHPKPLNTAVANSALTIATRMGMDVTLLCPTPDYILDERYMDWAAQNVAESGGSLQV 235
            W          + NS +  A +    + + CP           D  A+ +A++G  + +
Sbjct: 155 AWIGD----GNNMCNSYIEAAMQFDFQLRVACPEG--------FDPNAELLAKAGDRVSI 202

Query: 236 SHDIDSAYAGADVVYAKSWGALPFFGNWEPEKPIRDQYQHFIVDERKMALTNNGV-FSHC 294
             D   A AGA +V    W ++   G  E      + +    V+   + L +  V F HC
Sbjct: 203 VRDPKLAVAGAHLVSTDVWTSM---GQEEETARRLELFAPLQVNRALLDLADADVLFMHC 259

Query: 295 LPLRRNVKATDAVMDSPNCIAIDEAENRLHVQKAIMAALV 334
           LP  R  + +  ++D P  +A D+AENRLH QKA++  LV
Sbjct: 260 LPAHRGEEISMDLLDDPRSVAWDQAENRLHAQKALLEFLV 299


Lambda     K      H
   0.320    0.134    0.412 

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: 216
Number of extensions: 6
Number of successful extensions: 3
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: 339
Length of database: 306
Length adjustment: 28
Effective length of query: 311
Effective length of database: 278
Effective search space:    86458
Effective search space used:    86458
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: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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