GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argF' in Thioalkalivibrio halophilus HL17

Align N-acetylornithine carbamoyltransferase (EC 2.1.3.9) (characterized)
to candidate WP_024329362.1 B1A74_RS04880 ornithine carbamoyltransferase

Query= BRENDA::Q8P8J2
         (339 letters)



>NCBI__GCF_001995255.1:WP_024329362.1
          Length = 304

 Score =  138 bits (348), Expect = 2e-37
 Identities = 113/342 (33%), Positives = 164/342 (47%), Gaps = 50/342 (14%)

Query: 1   MSLKHFLNTQDWSRAELDALLTQAALFKRNKLGSE-----LKGKSIALVFFNPSMRTRTS 55
           M+ +HFL+  D S  E  A+L +A   KR     E     L+GK++ ++F   S RTR S
Sbjct: 1   MNPRHFLSFLDLSAEETRAVLHRAIELKRQLKAGEHHDDLLRGKTLGMIFEKSSTRTRVS 60

Query: 56  FELGAFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVLGRYVDLIGVRAFP 115
           FE+G  QLGG+A+ L P       +  LG        E I + ARVL R VD + +R + 
Sbjct: 61  FEVGMQQLGGNALFLSPR------DTQLGR------GEPIEDTARVLSRMVDCVMIRTY- 107

Query: 116 KFVDWSKDREDQVLKSFAKYSPVPVIN-METITHPCQELAHALALQEHFGTPDLRGKKYV 174
                    E + ++ FA++S VPVIN +  + HP Q LA      E+ G  D+RGK+  
Sbjct: 108 ---------EHEKVELFARHSSVPVINGLTDLEHPAQLLADLQTFFEYRG--DIRGKR-- 154

Query: 175 LTWTYHPKPLNTAVANSALTIATRMGMDVTLLCPTPDYILDERYMDWAAQNVAESGGSLQ 234
           + W          + +S +  A  +  ++   CP  DY  +   ++    +V        
Sbjct: 155 VAWIGD----GNNMCHSYMYAAHLLDFELMAACPE-DYEPESSVLEATRDHVT------- 202

Query: 235 VSHDIDSAYAGADVVYAKSWGALPFFGNWEPEKPIRDQ-YQHFIVDERKMALTN-NGVFS 292
           V+ D   A AGAD+V    W ++      E EK  R Q +  F VD+  M     N +F 
Sbjct: 203 VTRDAGEAAAGADLVVTDVWASM----GQEQEKSARRQAFAGFFVDQALMDRAQPNALFM 258

Query: 293 HCLPLRRNVKATDAVMDSPNCIAIDEAENRLHVQKAIMAALV 334
           HCLP  R  +    V++ P  +  DEAENRLH QKA+M  LV
Sbjct: 259 HCLPAHREEEVATDVLEGPQSVVWDEAENRLHAQKALMEFLV 300


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: 220
Number of extensions: 8
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 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