GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Halococcus hamelinensis 100A6

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_007691423.1 C447_RS04715 aspartate aminotransferase family protein

Query= reanno::WCS417:GFF4238
         (406 letters)



>NCBI__GCF_000336675.1:WP_007691423.1
          Length = 378

 Score =  219 bits (559), Expect = 8e-62
 Identities = 139/368 (37%), Positives = 194/368 (52%), Gaps = 17/368 (4%)

Query: 30  RGEGSRVWDQAGRELIDFAGGIAVNVLGHAHPALVGALTEQAHKLWHVSNVFTNEPALRL 89
           RGEG+ ++D  G E +D     A   LGH HPA+  A+ +Q  +L  V   +  +   R 
Sbjct: 15  RGEGAYLYDTDGTEYLDCGASYACTPLGHDHPAVNEAVHDQVDRLTFVQASYPVDARDRA 74

Query: 90  AHKLIDAT--FAERVFFCNSGAEANEAAFKLARRVAFDRFGSEKYEIIAALNSFHGRTLF 147
              L  A     E V+ CNSG EANEAA K AR        + + +I+A +  FHGRT+ 
Sbjct: 75  FDALAAAAPEGLENVWLCNSGTEANEAALKFARSA------TGRSKIVATMQGFHGRTMG 128

Query: 148 TVNVGGQSKYSDGFGPKITGITHVPYNDLDALKAAVSDKTCAVVLEPIQGEGGVLPAELA 207
            +     + Y D F P I  +  VPY D +AL  AV D+T AV++EPIQGEGG+      
Sbjct: 129 ALATTWNNDYRDPFEPLIGDVEFVPYGDSEALAEAVDDETAAVIVEPIQGEGGINVPTDG 188

Query: 208 YLQGARDLCDANNALLVFDEVQTGMGRSGHLFAYQHYGVTPDILTSAKSLGGGFPIAAML 267
           YL  AR+  +   A LVFDEVQTGMGR+G L+A Q  GV PD+LT+AK L  G P    L
Sbjct: 189 YLAAARECTEDAGAALVFDEVQTGMGRTGTLWASQQAGVVPDVLTTAKGLANGLPAGTAL 248

Query: 268 TTEALAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLAGVNAKHDLFKARLE-QIG 326
             + +A     G H  T+ G P+  A  +A +  +   EV +   A  +  +A L+  IG
Sbjct: 249 CADWIADD--HGPHNATFSGGPVVSAAVDATVSTLVEEEVPSNAGAVGEYLRAGLDAAIG 306

Query: 327 KQYGIFTEVRGMGLLLGCVLSDAFKGKAKDVFNAAEKENLMILQAGPDVVRFAPSLVVED 386
                  E+RG GL++G    +  +G  + + + A   NL+ L AG  VVR  P LV+++
Sbjct: 307 DD---VREIRGEGLMIGI---EVKRGANRALRDLALDSNLLALPAGRSVVRLLPPLVLDE 360

Query: 387 ADIKEGLD 394
            D  E +D
Sbjct: 361 DDADEVVD 368


Lambda     K      H
   0.320    0.137    0.400 

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: 391
Number of extensions: 17
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: 406
Length of database: 378
Length adjustment: 31
Effective length of query: 375
Effective length of database: 347
Effective search space:   130125
Effective search space used:   130125
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 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