GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Thermomonospora curvata DSM 43183

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_012852504.1 TCUR_RS10655 acetylornithine transaminase

Query= BRENDA::O30508
         (406 letters)



>NCBI__GCF_000024385.1:WP_012852504.1
          Length = 401

 Score =  282 bits (722), Expect = 1e-80
 Identities = 161/376 (42%), Positives = 220/376 (58%), Gaps = 12/376 (3%)

Query: 18  VPNYAPAAFIPVRGEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWHV 77
           +PNY       V G+G  V D  G+E +DF  GIAV+SLGH HPAL++A+T Q   I H 
Sbjct: 15  MPNYGLPPVALVSGQGCLVRDADGKEYLDFIAGIAVSSLGHGHPALIEAVTAQVGAIAHT 74

Query: 78  SNVFTNEPALRLA---RKLVDATFAE-RVFLANSGAEANEAAFKLARRYANDVYGPQKYE 133
           SN+F NEP ++LA   R+L+    A+ RVFL+NSG EANE A KLA +YA      ++  
Sbjct: 75  SNLFVNEPEVQLAERLRRLLGEHGAKARVFLSNSGTEANECALKLAIKYAK---AHERTY 131

Query: 134 IIAASNSFHGRTLFTVNVGGQPKYSDGFGPKFEGITHVPYNDLEALKAAISDKTCAVVLE 193
            +AA N FHGRT+  +++ G+    + FGP    +  VPY D +AL+ A++ +  AV LE
Sbjct: 132 FVAAENGFHGRTMGALSLTGKHAIREPFGPYAIDVRFVPYGDADALRQAVTPQCAAVFLE 191

Query: 194 PIQGEGGVLPAQQAYLEGARKLCDEHNALLVFDEVQSGMGRVGELFAYMHYGVVPDILSS 253
           P  GEGGV+P    YL  AR +CD+  ALLV DE+QS +GR G  FA+ H GV PDIL+ 
Sbjct: 192 PTLGEGGVVPPPDGYLSAARDICDQSGALLVIDEIQSAIGRTGTWFAHQHEGVRPDILTL 251

Query: 254 AKSLGGGFPIGAMLTTGEIAKHLSVGTHGTTYGGNPLASAVAEAALDVINTPEVLDGVKA 313
           AK LGGG PIGA +  G   +  + G HG+T+GGNP+++A A A L  I    +LD V  
Sbjct: 252 AKGLGGGLPIGACIGFGPYGELFAKGDHGSTFGGNPVSAAAALAVLRTIEAEGLLDHVTK 311

Query: 314 KHERFKSRLQKIGQEYGIFDEIRGMGLLIGAALTDEWKGKARDVLNAAEKEAVMVLQASP 373
                K  L  I   + +   +RG GL +G  LT+     A  V  AA     +V    P
Sbjct: 312 VGALLKEGLSAIA--HPLLKSVRGRGLWLGLVLTEP---LAAQVEAAARDAGFLVNAVQP 366

Query: 374 DVVRFAPSLVIDDAEI 389
           +V+R AP L++   ++
Sbjct: 367 NVIRLAPPLIVTAEQV 382


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: 476
Number of extensions: 32
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: 406
Length of database: 401
Length adjustment: 31
Effective length of query: 375
Effective length of database: 370
Effective search space:   138750
Effective search space used:   138750
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 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