GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argF' in Herbaspirillum seropedicae SmR1

Align N-acetylornithine carbamoyltransferase (EC 2.1.3.9) (characterized)
to candidate HSERO_RS07185 HSERO_RS07185 ornithine carbamoyltransferase

Query= BRENDA::Q8P8J2
         (339 letters)



>FitnessBrowser__HerbieS:HSERO_RS07185
          Length = 304

 Score =  118 bits (295), Expect = 2e-31
 Identities = 101/341 (29%), Positives = 157/341 (46%), Gaps = 49/341 (14%)

Query: 1   MSLKHFLNTQDWSRAELDALLTQAALFKRNKLGSE----LKGKSIALVFFNPSMRTRTSF 56
           M++KH+L   D++  E + ++ ++ + KR     E    L  +++ +VF   S RTR SF
Sbjct: 1   MAIKHYLQFSDFTLDEYEYVIERSRVIKRKFKNYEPHHTLADRTLVMVFEKNSTRTRLSF 60

Query: 57  ELGAFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVLGRYVDLIGVRAFPK 116
           E G  Q+GG A+ L         +  LG        E + + A+V+ R  D+I +R + +
Sbjct: 61  EAGMHQMGGAAIYLNTR------DSQLGR------GEPVEDAAQVMSRMCDVIMIRTYGQ 108

Query: 117 FVDWSKDREDQVLKSFAKYSPVPVIN-METITHPCQELAHALALQEHFGTPDLRGKKYVL 175
                     ++++ FAK+S VPVIN +    HPCQ LA      EH G+  ++GK  ++
Sbjct: 109 ----------EIIERFAKHSRVPVINGLTNEQHPCQVLADVFTYIEHHGS--IQGK--IV 154

Query: 176 TWTYHPKPLNTAVANSALTIATRMGMDVTLLCPTPDYILDERYMDWAAQNVAESGGSLQV 235
            W      +      S L  A   G  V +  P   Y +D   +    +N          
Sbjct: 155 AWVGDANNM----LYSWLQAAEVFGFHVNVSTPK-GYDIDPAQVSPGNKNYTFFADPADA 209

Query: 236 SHDIDSAYAGADVVYAKSWGALPFFGNWEPEKPIR-DQYQHFIVDERKMALTN-NGVFSH 293
             D       AD+V    W ++ F    E E   R   +  +IVD+ KMA    + +F H
Sbjct: 210 CQD-------ADLVTTDVWTSMGF----EAENNARLKAFDGWIVDQAKMARAKKDALFMH 258

Query: 294 CLPLRRNVKATDAVMDSPNCIAIDEAENRLHVQKAIMAALV 334
           CLP  R  +    V+D P  +  +EAENRLHVQKA++  LV
Sbjct: 259 CLPAHRGEEVAAEVIDGPQSVVWEEAENRLHVQKALLEYLV 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: 238
Number of extensions: 10
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: 339
Length of database: 304
Length adjustment: 28
Effective length of query: 311
Effective length of database: 276
Effective search space:    85836
Effective search space used:    85836
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