GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Azoarcus olearius BH72

Align Succinylornithine transaminase; SOAT; EC 2.6.1.81; Succinylornithine aminotransferase (uncharacterized)
to candidate WP_011764928.1 AZO_RS06045 acetylornithine transaminase

Query= curated2:Q3Z295
         (406 letters)



>NCBI__GCF_000061505.1:WP_011764928.1
          Length = 392

 Score =  290 bits (743), Expect = 4e-83
 Identities = 164/361 (45%), Positives = 220/361 (60%), Gaps = 5/361 (1%)

Query: 27  RGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPELREALNEQASKFWHTGNGYTNEPVLRL 86
           RGEGS L+D QGK Y+DF  G AVN LGH+  E+R+A+  QA K  +    + N P++ L
Sbjct: 24  RGEGSWLYDAQGKAYLDFVQGWAVNCLGHSPAEVRDAIVAQAGKLINPSPAFYNGPMIEL 83

Query: 87  AKKLIDATFADRVFFCNSGAEANEAALKLARKFAH-DRYGSHKSGIVAFKNAFHGRTLFT 145
           A  L      DRVFF N+GAEANE A+KLARK+    R G+++  I+ F+++FHGRTL T
Sbjct: 84  AGLLTAHCSLDRVFFANTGAEANEGAIKLARKWGRLHRNGAYQ--IITFEHSFHGRTLAT 141

Query: 146 VSAGGQPAYSQDFAPLPPDIRHAAYNDINSASALIDDATCAVIVEPIQGEGGVVPASNAF 205
           +SA G+  +   FAP  P    A  ND+ S  ALI   T AV++EP+QGEGGV+PA+  F
Sbjct: 142 MSASGKAGWDTLFAPQVPGFPKARLNDLESVKALIGPETVAVMLEPVQGEGGVIPAAPEF 201

Query: 206 LQGLRELCDRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLTTAKALGGGFPVGALLT 265
           LQ LR L   H  LLI DEVQ+G+GRTG L+A+ H G+ PD++T  K +GGG P+ ALL 
Sbjct: 202 LQALRALTREHGILLIVDEVQSGMGRTGRLFAHQHAGIEPDIMTLGKGIGGGVPLSALLA 261

Query: 266 TEECASVMTVGTHGTTYGGNPLASAVAGKVLELINTPEMLNGVKQRHDWFVERLNTINHR 325
           T E  S    G  G TY GNPL +A    V+  +  P  L+ V  R D+   RL  +  +
Sbjct: 262 T-EAVSCFEAGDQGGTYNGNPLMTAAGIAVMRRLTAPGFLDEVLARGDYLAARLRELVAK 320

Query: 326 YGLFSEVRGLGLLIGCVLNADYAGQAKQISQEAAKAGVMVLIAGGNVVRFAPALNVSEEE 385
             L  E RG GLL   VL++D A    + + E A  G+++     N++RF P+L VSE E
Sbjct: 321 RHLVGE-RGSGLLRALVLDSDRAPAIVKAALEGAPTGLLLNAPRPNLLRFMPSLTVSEAE 379

Query: 386 V 386
           +
Sbjct: 380 I 380


Lambda     K      H
   0.319    0.136    0.408 

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: 443
Number of extensions: 21
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: 392
Length adjustment: 31
Effective length of query: 375
Effective length of database: 361
Effective search space:   135375
Effective search space used:   135375
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.

Links

Downloads

Related tools

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