GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Desulfarculus baarsii DSM 2075

Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_013257174.1 DEBA_RS01715 isocitrate/isopropylmalate family dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000143965.1:WP_013257174.1
          Length = 330

 Score =  322 bits (825), Expect = 8e-93
 Identities = 174/330 (52%), Positives = 225/330 (68%), Gaps = 4/330 (1%)

Query: 1   MHKICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALD 60
           ++ I VI GDGIG EVV A I VLEATGL + F   EAGD+     G+ALP+ T++ AL 
Sbjct: 5   IYDIAVIGGDGIGPEVVEAEIAVLEATGLAWNFSSYEAGDDCLASRGQALPQATLDGALA 64

Query: 61  CDAVLFGAAGETAADVIVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENTEGLYK 120
             AV+FGAAG +AADVI++LR  L T+ N+RP  AYKGV CL P  D +IVRENTE LY 
Sbjct: 65  AQAVIFGAAGVSAADVILRLRAELGTFVNLRPSVAYKGVNCLHPQTDMMIVRENTECLYA 124

Query: 121 GIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVLKLTDGL 180
           GIEA++   +  ATRVIT +A  RI  +A   AR+    GK  KVT  HKANVL+ TDG 
Sbjct: 125 GIEAQLTPEVVTATRVITSQASTRIVNYALEWARQAG--GK--KVTAVHKANVLRKTDGH 180

Query: 181 FKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAGTVGGL 240
           F +     A ++ D+  E+  +D++ M +  +P+ F V+VT+NLFGDILSD AAG +GGL
Sbjct: 181 FLQCCRAAARQFPDVPYEEALVDSVAMRMAMRPEEFQVIVTTNLFGDILSDLAAGLIGGL 240

Query: 241 GLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADKVEKAL 300
           G+ PSAN+G  H LFEPVHG+APDIAG+  ANP+A IL   ++LR+LG+ + A +VEKA+
Sbjct: 241 GMCPSANLGQAHALFEPVHGTAPDIAGQGKANPSAAILCGAMLLRHLGQEQWAARVEKAV 300

Query: 301 EEVLALGLTTPDLGGNLNTFEMAEEVAKRV 330
            + +A G  T DLGG L T EMA  V  R+
Sbjct: 301 ADCVADGQATSDLGGKLRTMEMARAVIDRL 330


Lambda     K      H
   0.318    0.138    0.390 

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: 314
Number of extensions: 15
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: 333
Length of database: 330
Length adjustment: 28
Effective length of query: 305
Effective length of database: 302
Effective search space:    92110
Effective search space used:    92110
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: 49 (23.5 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