GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Calditerrivibrio nitroreducens DSM 19672

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_013450865.1 CALNI_RS03705 aspartate aminotransferase family protein

Query= BRENDA::O30508
         (406 letters)



>NCBI__GCF_000183405.1:WP_013450865.1
          Length = 386

 Score =  317 bits (811), Expect = 5e-91
 Identities = 163/374 (43%), Positives = 240/374 (64%), Gaps = 5/374 (1%)

Query: 29  VRGEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWHVSNVFTNEPALR 88
           V+G+   ++D++G++ +DFA GIAVT+LGH++  + + +  Q+  + H SN++ N     
Sbjct: 16  VKGDYFYLFDENGKKYVDFATGIAVTNLGHSNKEIAEIICRQSATLMHTSNLYKNPIQEE 75

Query: 89  LARKLVDATFAERVFLANSGAEANEAAFKLARRYANDVYGPQKYEIIAASNSFHGRTLFT 148
           +A+ + D +F  +VF  NSGAEANEAA KLAR Y N  +  ++Y+II   NSFHGRT  T
Sbjct: 76  VAQIISDLSFGCKVFFCNSGAEANEAALKLARIYGNKKHNGKRYKIITMVNSFHGRTFAT 135

Query: 149 VNVGGQPKYSDGFGPKFEGITHVPYNDLEALKAAISDKTCAVVLEPIQGEGGVLPAQQAY 208
           +   GQ K   GF P  + I H+P+ND++A + AI  +T AVV+E IQGEGGV+PA++ Y
Sbjct: 136 LAATGQEKVKKGFEPTLDFIKHIPFNDIDAFEKAIEPETVAVVMEVIQGEGGVIPAKEGY 195

Query: 209 LEGARKLCDEHNALLVFDEVQSGMGRVGELFAYMHYGVVPDILSSAKSLGGGFPIGAMLT 268
           L+  R++C E + LL+FDEVQ+G+GR GE+F Y  Y V PDI + AK+LG GFPIGAM+ 
Sbjct: 196 LDAVRRICFEKDILLIFDEVQTGIGRTGEVFGYQLYDVKPDIFTLAKALGNGFPIGAMVA 255

Query: 269 TGEIAKHLSVGTHGTTYGGNPLASAVAEAALDVINTPEVLDGVKAKHERFKSRLQKIGQE 328
             EIA++LS GTH +T+GGN L  A+A+  L+ ++    LD VK K    K++L+ I   
Sbjct: 256 KTEIAEYLSPGTHASTFGGNYLGCAIAKYVLETVSDRSFLDSVKEKGNYLKNKLKTI--- 312

Query: 329 YGIFDEIRGMGLLIGAALTDEWKGKARDVLNAAEKEAVMVLQASPDVVRFAPSLVIDDAE 388
           +G   EIRG G++IG  L D       D ++ A K  V+ + A  + VR  P+L I    
Sbjct: 313 FGDMGEIRGEGMMIGVRLIDSI--SLSDFIDRAHKNGVLTVPAGDNTVRIYPALNISYDV 370

Query: 389 IDEGLERFERAVAK 402
           ++EGLE   + + +
Sbjct: 371 LNEGLELINKTIGE 384


Lambda     K      H
   0.318    0.135    0.394 

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: 389
Number of extensions: 14
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: 386
Length adjustment: 31
Effective length of query: 375
Effective length of database: 355
Effective search space:   133125
Effective search space used:   133125
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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