GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argF' in Sinorhizobium meliloti 1021

Align N-acetylornithine carbamoyltransferase (EC 2.1.3.9) (characterized)
to candidate SMc02137 SMc02137 ornithine carbamoyltransferase

Query= BRENDA::Q8P8J2
         (339 letters)



>FitnessBrowser__Smeli:SMc02137
          Length = 303

 Score =  144 bits (363), Expect = 3e-39
 Identities = 109/338 (32%), Positives = 164/338 (48%), Gaps = 45/338 (13%)

Query: 4   KHFLNTQDWSRAELDALLTQAALFKR-NKLGSE---LKGKSIALVFFNPSMRTRTSFELG 59
           +HFL+    +  +L  ++  A + K   K G+    L GK +A++F  PS RTR SF++G
Sbjct: 3   RHFLDLSAMTATDLRTIIDDARVRKSATKAGTAEKPLAGKMLAMIFEKPSTRTRVSFDVG 62

Query: 60  AFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVLGRYVDLIGVRAFPKFVD 119
             QLGG  + L             GT M     E I + A+VL RYVD I +R       
Sbjct: 63  MRQLGGETLFLS------------GTEMQLGRAETIGDTAKVLSRYVDAIMIRT------ 104

Query: 120 WSKDREDQVLKSFAKYSPVPVIN-METITHPCQELAHALALQEHFGTPDLRGKKYVLTWT 178
                + + L   A+++ VPVIN +   THPCQ +A  L  +EH G   ++GK   + WT
Sbjct: 105 ----TDHRRLLEMAEHATVPVINGLTDDTHPCQIMADILTFEEHRGP--VKGK--TIAWT 156

Query: 179 YHPKPLNTAVANSALTIATRMGMDVTLLCPTPDYILDERYMDWAAQNVAESGGSLQVSHD 238
                +  ++   +     RM M V L     D     ++++WA  N AE    + +SH+
Sbjct: 157 GDGNNVLHSLIEGSARFGYRMNMAVPLGSEPHD-----KFLNWARNNGAE----VLLSHE 207

Query: 239 IDSAYAGADVVYAKSWGALPFFGNWEPEKPIRDQYQHFIVDERKMA-LTNNGVFSHCLPL 297
            + A AGA  V   +W ++    N E      + +Q + V+   M     + +F HCLP 
Sbjct: 208 AEQAVAGAHCVVTDTWISM----NQEHRARGHNVFQPYQVNGALMKHAAPDALFMHCLPA 263

Query: 298 RRNVKATDAVMDSPNCIAIDEAENRLHVQKAIMAALVG 335
            R  + TD V+D P  +  DEAENRLH QK+I+A  +G
Sbjct: 264 HRGEEVTDEVIDGPQSVVFDEAENRLHAQKSILAWCMG 301


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: 265
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: 303
Length adjustment: 28
Effective length of query: 311
Effective length of database: 275
Effective search space:    85525
Effective search space used:    85525
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.

Links

Downloads

Related tools

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