GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Desulfuromusa kysingii DSM 7343

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_092344193.1 BLU87_RS01675 acetylornithine transaminase

Query= reanno::pseudo1_N1B4:Pf1N1B4_3440
         (406 letters)



>NCBI__GCF_900107645.1:WP_092344193.1
          Length = 397

 Score =  342 bits (878), Expect = 9e-99
 Identities = 173/370 (46%), Positives = 234/370 (63%), Gaps = 4/370 (1%)

Query: 21  YAPAAFIPVRGAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVSNV 80
           Y     +   G G  + D  G+  +DF  G+AVN LGH HP +VAAL EQA KL H SN 
Sbjct: 19  YGRFPLVAASGKGCWLTDIDGKRYLDFLAGVAVNSLGHCHPKVVAALQEQAAKLLHCSNY 78

Query: 81  FTNEPALRLAHKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEIVAALNS 140
           +     + LA  L + +F +RVFFCNSGAEANEAA KL R+ + D +GT+++EI+ A++S
Sbjct: 79  YHIPQQIELAEILCEHSFGDRVFFCNSGAEANEAALKLVRKYSADTYGTDRFEIITAIDS 138

Query: 141 FHGRTLFTVNVGGQSKYSDGFGPKITGITHVPYNDLAALKAAVSDKTCAVVLEPIQGEGG 200
           FHGRTL T++  GQ +   GF P I+G  +VP+ D+AALK A+  KTCA+++EPIQGEGG
Sbjct: 139 FHGRTLATISATGQDRIQSGFAPLISGFKYVPFGDIAALKTAIGPKTCAIMMEPIQGEGG 198

Query: 201 VLPAELSYLQGARELCDAHNALLVFDEVQTGMGRSGKLFAYQHYGVTPDILTSAKSLGGG 260
           +      YLQ ARELCD HN LL+FDE+Q G+GR+GKLFAY+H  V PD++T AK+L  G
Sbjct: 199 INVPPQGYLQAARELCDKHNLLLIFDEIQVGLGRTGKLFAYEHDNVEPDVMTLAKALAAG 258

Query: 261 FPIAAMLTTEDLAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLNGVNAKHDKFKT 320
            PI AM+  E  A  L  GTHG+T+GGNPL  A   A + V+    +++   A  +  K 
Sbjct: 259 PPIGAMIAREKYATALSPGTHGSTFGGNPLLTAAGVAAMKVLLEDHIIDNCVAMGNYLKA 318

Query: 321 RLEQIGEKYGLFTEVRGLGLLLGCVLSDAWKGKAKDIFNAAEREGLMILQAGPDVIRFAP 380
           +LEQ+  KY     +RG GL+LG  L+     +  +I   A + GL+I      V+RF P
Sbjct: 319 QLEQLQNKYTFIKNIRGRGLILGMELT----FEGAEIVKTALQRGLLINCTAGKVLRFVP 374

Query: 381 SLVVEDADID 390
            L+V   +ID
Sbjct: 375 PLIVTQDEID 384


Lambda     K      H
   0.320    0.136    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: 414
Number of extensions: 19
Number of successful extensions: 2
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: 397
Length adjustment: 31
Effective length of query: 375
Effective length of database: 366
Effective search space:   137250
Effective search space used:   137250
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