GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Malonomonas rubra DSM 5091

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_072909607.1 BUB13_RS15120 aspartate aminotransferase family protein

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



>NCBI__GCF_900142125.1:WP_072909607.1
          Length = 401

 Score =  325 bits (834), Expect = 1e-93
 Identities = 170/367 (46%), Positives = 226/367 (61%), Gaps = 4/367 (1%)

Query: 31  GAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVSNVFTNEPALRLA 90
           G G  + D  G+  +DF  G+AVN LGH HP +V A+ EQA KL H SN +     + LA
Sbjct: 29  GDGCWLLDVDGKRYLDFLAGVAVNNLGHCHPKVVKAIQEQAGKLLHCSNFYHIPQQIELA 88

Query: 91  HKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEIVAALNSFHGRTLFTVN 150
             L   +F +RVFFCNSG EANEAA KLAR+ +++  G E+ E++ A+ SFHGRTL  ++
Sbjct: 89  ELLCTHSFGDRVFFCNSGVEANEAAIKLARKYSYENHGKERNEVITAVASFHGRTLAGIS 148

Query: 151 VGGQSKYSDGFGPKITGITHVPYNDLAALKAAVSDKTCAVVLEPIQGEGGVLPAELSYLQ 210
             GQ K  +GF P + G  HVP+ D  A++AAV   TCA++LEP+QGEGGV      YLQ
Sbjct: 149 ATGQDKVKEGFAPMLPGFKHVPFGDFEAMRAAVGPNTCAIMLEPVQGEGGVNIPPAGYLQ 208

Query: 211 GARELCDAHNALLVFDEVQTGMGRSGKLFAYQHYGVTPDILTSAKSLGGGFPIAAMLTTE 270
             RELCD +N LL+FDEVQ G GR+G LFAYQ  GV PDI+T AK+L GG PI AM++ E
Sbjct: 209 SIRELCDENNLLLIFDEVQVGCGRTGSLFAYQQEGVEPDIMTLAKALAGGPPIGAMISRE 268

Query: 271 DLAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLNGVNAKHDKFKTRLEQIGEKYG 330
             A  L  GTHG+T+GGNPL  + A A + V     VL       D  + +LE++ EKY 
Sbjct: 269 KHAGALGPGTHGSTFGGNPLLASAALAAMKVYLEDGVLENCRKTGDYLRAKLEELQEKYD 328

Query: 331 LFTEVRGLGLLLGCVLSDAWKGKAKDIFNAAEREGLMILQAGPDVIRFAPSLVVEDADID 390
              EVRG GL++G  L+ A      ++   A   GL+I      V+RF P L+++  +ID
Sbjct: 329 FVVEVRGRGLIIGMELNIA----GGEMVKTALERGLLINCTVDKVLRFVPPLIIDTDEID 384

Query: 391 AGLDRFE 397
             ++  E
Sbjct: 385 QMIEILE 391


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: 411
Number of extensions: 18
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: 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 ( 7.4 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