GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Acidovorax sp. GW101-3H11

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate Ac3H11_375 Tartrate dehydrogenase (EC 1.1.1.93) @ Tartrate decarboxylase (EC 4.1.1.73) @ D-malic enzyme (EC 1.1.1.83)

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_375
          Length = 364

 Score =  228 bits (580), Expect = 2e-64
 Identities = 142/361 (39%), Positives = 205/361 (56%), Gaps = 29/361 (8%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAE-AGWETFERRGTSVPEETVE 57
           +RI ++ GDGIG EV+P   RVL+      G+ L F   + + W+ +E+ G  +P+   E
Sbjct: 4   HRIAVVAGDGIGKEVMPEGLRVLDVAARKFGIDLHFDHFDFSSWDYYEKHGKMLPDNWKE 63

Query: 58  KILSCHATLFGAATSPTRKVP--GFFGAIRYLRRRLDLYANVRPAKSRP---VPGSR--- 109
           +I S  A  FGA   P +       +G++   RR  D Y N+RPA+  P    P  R   
Sbjct: 64  QIGSHEAIYFGAVGWPEKIADHVSLWGSLLLFRREFDQYINLRPARLMPGVIAPVVRRDG 123

Query: 110 ----PG-VDLVIVRENTEGLYVEQERRYLD-----VAIADAVISKKASERIGRAALRIAE 159
               PG +D++IVRENTEG Y     R  +     + + + V+S+   +R+ + A  +A+
Sbjct: 124 SPRLPGEIDMLIVRENTEGEYSSIGGRMYEGTPREIVMQETVMSRHGVDRVLKFAFDLAQ 183

Query: 160 GRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDV 219
            RP+K L  A K+N + +T   + + V E+AK +P V V    +D      V RP+ FDV
Sbjct: 184 SRPKKHLTSATKSNGIAITMPYWDERVAEMAKSYPDVKVDKFHIDILTAHFVQRPDFFDV 243

Query: 220 IVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDT---TAVFEPVHGSAPDIAGKGIANPTA 276
           +V +NL GDILSDL     G +G+APS N+  T    ++FEPVHGSAPDIAG+GIANP  
Sbjct: 244 VVASNLFGDILSDLGPACTGTIGIAPSANLNPTRTMPSLFEPVHGSAPDIAGQGIANPIG 303

Query: 277 AILSAAMMLDYLGEKEAAKRVEKAVDLVLE---RGPRTPDLGGDATTEAFTEAVVEALKS 333
            I   AMMLD+LG + A   V  A++ VL+    GPRTPDLGG + T+   +A+ EAL +
Sbjct: 304 QIWCGAMMLDFLGYRAAHDAVLAAIEAVLDPQSGGPRTPDLGGKSGTQDVGKAIAEALSA 363

Query: 334 L 334
           +
Sbjct: 364 V 364


Lambda     K      H
   0.319    0.137    0.391 

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: 341
Number of extensions: 17
Number of successful extensions: 7
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: 334
Length of database: 364
Length adjustment: 29
Effective length of query: 305
Effective length of database: 335
Effective search space:   102175
Effective search space used:   102175
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 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