GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Methylomonas methanica MC09

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_013819183.1 METME_RS12875 acetylornithine transaminase

Query= reanno::Koxy:BWI76_RS11670
         (406 letters)



>NCBI__GCF_000214665.1:WP_013819183.1
          Length = 390

 Score =  296 bits (758), Expect = 7e-85
 Identities = 162/376 (43%), Positives = 227/376 (60%), Gaps = 7/376 (1%)

Query: 14  MMPVYAPAAFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPRLVKALTEQAGKFWH 73
           +MP YA       RGEG+ LWD  GK Y+D   GIAV  LGHAHP + +AL +Q+    H
Sbjct: 5   IMPTYARQTVTFDRGEGAWLWDSNGKRYLDALAGIAVCNLGHAHPAVHQALCKQSQTLIH 64

Query: 74  TGNGYTNEPVLRLAKQLIDATFADRVFFCNSGAEANEAALKLARKYAHDRFGSEKSGIVA 133
           T N Y  +    LA +L   +  D VFFCNSGAEANEAA+K+ARKY H++ G +   I+ 
Sbjct: 65  TSNLYGVKLQAELADKLCRLSGMDNVFFCNSGAEANEAAIKIARKYGHEQ-GIDAPVILT 123

Query: 134 FKNAFHGRTLFTVSAGGQPAYSQDFAPLPPQIQHAIYNDLDSAKALI--DDNTCAVIVEP 191
              +FHGRT+  +SA G     Q FAPL P   H  YN++D+  + I  D N  A++VEP
Sbjct: 124 MDKSFHGRTMGALSATGNTKIKQGFAPLLPGFVHVPYNNIDAIISAIHADKNIVAILVEP 183

Query: 192 MQGEGGVVPADADFLRGLRELCDAHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLSTA 251
           +QGEGGV   DAD+L  +R LCD H  LL+ DE+QTG+GRTGE  AY    + PD+ + A
Sbjct: 184 VQGEGGVNIPDADYLNRIRALCDEHQLLLMLDEIQTGIGRTGEFLAYQRNQILPDVCTLA 243

Query: 252 KALGGGFPIGALLASERCASVMTVGTHGTTYGGNPLACAVAGEVFATINTREVLNGVKQR 311
           KALG G PIGA +A  + A+++T G HG+T+GGNPLAC+ A  V  T+ + +++    ++
Sbjct: 244 KALGNGVPIGACMARGKAAAILTAGNHGSTFGGNPLACSAALAVLDTLCSTDLIADADRK 303

Query: 312 HQWFCERLNAINARYGLFKEIRGLGLLIGCVLKDEYAGKAKAISNQAAEEGLMILIAGAN 371
            +  C+ +            IR LGL+IG  L D   G+   +  +A E+GL+I +   N
Sbjct: 304 GKRICDAVTRQLEGNPHIVSIRHLGLMIGIEL-DAPCGE---LVGKALEQGLLINVTADN 359

Query: 372 VVRFAPALIISEDEVN 387
            +R  P L+I + +++
Sbjct: 360 TIRLLPPLLIDDAQID 375


Lambda     K      H
   0.321    0.137    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: 422
Number of extensions: 17
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: 406
Length of database: 390
Length adjustment: 31
Effective length of query: 375
Effective length of database: 359
Effective search space:   134625
Effective search space used:   134625
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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