GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argF' in Malonomonas rubra DSM 5091

Align N-acetylornithine carbamoyltransferase (EC 2.1.3.9) (characterized)
to candidate WP_072909608.1 BUB13_RS15125 ornithine carbamoyltransferase

Query= BRENDA::Q8P8J2
         (339 letters)



>NCBI__GCF_900142125.1:WP_072909608.1
          Length = 303

 Score =  150 bits (380), Expect = 3e-41
 Identities = 116/341 (34%), Positives = 168/341 (49%), Gaps = 46/341 (13%)

Query: 3   LKHFLNTQDWSRAELDALLTQAALFKRNKLGSE----LKGKSIALVFFNPSMRTRTSFEL 58
           +K FL   DWS A+L+ +   A   K  +   E    L+G+++ ++F   S RTR SFE+
Sbjct: 2   MKDFLCLSDWSLADLEKMFALAKELKAKQKAGEAHKLLEGQTLGMLFEKSSTRTRVSFEV 61

Query: 59  GAFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVLGRYVDLIGVRAFPKFV 118
           G FQLGGHA+ L  G      +   G        E I + ARV+GRY D I +R + +  
Sbjct: 62  GMFQLGGHALFLSSGNT----QMGRG--------EPIKDTARVMGRYCDGIMIRTYSQ-- 107

Query: 119 DWSKDREDQVLKSFAKYSPVPVIN-METITHPCQELAHALALQEHFGTPDLRGKKYVLTW 177
                     ++ FA+Y   PVIN +  + HPCQ +A  + +QEH    D R  KY   W
Sbjct: 108 --------AAVEEFAEYCDAPVINGLTDMYHPCQIMADLMTVQEH--KEDYRNLKYC--W 155

Query: 178 TYHPKPLNTAVANSALTIATRMGMDVTLLCPTPDYILDERYMDWAAQNVAESGGSLQVSH 237
                     +ANS +  A   G ++ +  P   Y  D   +  A +    +G  L  ++
Sbjct: 156 IGD----GNNMANSWINAAAIFGFELRVATPK-GYEADAAVIARAEK----AGAKLIFTN 206

Query: 238 DIDSAYAGADVVYAKSWGALPFFGNWEPEKPIRDQYQHFIVDER--KMALTNNGVFSHCL 295
           D   A AGADV+    W ++   G  E +      +  F ++    KMA  +  V  HCL
Sbjct: 207 DPKEAAAGADVLNTDVWASM---GQEEEQAEREKAFVGFQINSELVKMAAADC-VVMHCL 262

Query: 296 PLRRNVKATDAVMDSPNCIAIDEAENRLHVQKAIMAALVGQ 336
           P  R+ + TD V++ PN I  DEAENRLHVQKAIMA+L+ +
Sbjct: 263 PAHRDEEITDEVIEGPNSIIFDEAENRLHVQKAIMASLMAK 303


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: 13
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: 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 Jul 25 2024. The underlying query database was built on Jul 25 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