GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Desulfobacca acetoxidans DSM 11109

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_013707407.1 DESAC_RS12335 acetylornithine transaminase

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



>NCBI__GCF_000195295.1:WP_013707407.1
          Length = 412

 Score =  355 bits (911), Expect = e-102
 Identities = 174/376 (46%), Positives = 244/376 (64%), Gaps = 4/376 (1%)

Query: 15  QVMVPNYAPAAFIPVRGAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKL 74
           + ++  YA    + +RG G R+WD  G+E +DF  GIAV  LGHAHPA+  A+  Q   L
Sbjct: 30  RTLMNTYARQPMVLMRGQGVRLWDLDGKEYLDFLAGIAVCNLGHAHPAITEAVCRQVQDL 89

Query: 75  WHVSNVFTNEPALRLAHKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEI 134
            HVSN++   P ++LA +LV+ +FA+RVFFCNSGAEANE A KL RR +  +FG ++Y+I
Sbjct: 90  VHVSNLYHTIPQIKLAERLVELSFADRVFFCNSGAEANEGAIKLCRRYSWQKFGPDRYKI 149

Query: 135 VAALNSFHGRTLFTVNVGGQSKYSDGFGPKITGITHVPYNDLAALKAAVSDKTCAVVLEP 194
           + A NSFHGRTL T++  GQ K+  GF P + G   VP+ND AAL+AA+ ++TC V+LEP
Sbjct: 150 ICAANSFHGRTLATLSATGQEKFWQGFAPLLPGFVFVPFNDPAALEAAIDNQTCGVLLEP 209

Query: 195 IQGEGGVLPAELSYLQGARELCDAHNALLVFDEVQTGMGRSGKLFAYQHYGVTPDILTSA 254
           +QGEGGV      Y    R LCD HN LL+ DE+Q G+GR+G+LFA++H+G+TPDI+T A
Sbjct: 210 VQGEGGVKIPTADYFPEVRNLCDKHNLLLILDEIQVGLGRTGRLFAHEHFGITPDIMTLA 269

Query: 255 KSLGGGFPIAAMLTTEDLAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLNGVNAK 314
           K L  G PI A+L TE++A   V GTH +T+GG P+  A A  V++++  P+ L  V AK
Sbjct: 270 KGLANGLPIGALLVTEEVAAGFVPGTHASTFGGGPVVTAAALTVLEILAQPDFLAEVKAK 329

Query: 315 HDKFKTRLEQIGEKYGLFTEVRGLGLLLGCVLSDAWKGKAKDIFNAAEREGLMILQAGPD 374
            + F   L Q+  ++    EVRGLGL+LG  +     G    + ++   +G +I     +
Sbjct: 330 GEYFLNGLRQLQPRHRFIQEVRGLGLILGIEID----GDGVPLVDSCREKGALINCTQGN 385

Query: 375 VIRFAPSLVVEDADID 390
           V+RF P LVV   +ID
Sbjct: 386 VLRFLPPLVVSREEID 401


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: 17
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: 412
Length adjustment: 31
Effective length of query: 375
Effective length of database: 381
Effective search space:   142875
Effective search space used:   142875
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