GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Methylomonas methanica MC09

Align Homoisocitrate dehydrogenase; HICDH; Homo(2)-isocitrate/homo(3)-isocitrate dehydrogenase; Isohomocitrate dehydrogenase; IHDH; NAD-dependent threo-isohomocitrate dehydrogenase; EC 1.1.1.87; EC 1.1.1.- (characterized)
to candidate WP_013817575.1 METME_RS04395 3-isopropylmalate dehydrogenase

Query= SwissProt::Q58991
         (347 letters)



>NCBI__GCF_000214665.1:WP_013817575.1
          Length = 368

 Score =  181 bits (460), Expect = 2e-50
 Identities = 134/374 (35%), Positives = 203/374 (54%), Gaps = 42/374 (11%)

Query: 3   KVCVIEGDGIGKEVIPEAIKILNELGE-----FEIIKGEAGLECLKKYGNALPEDTIEKA 57
           K+ V+ GDGIG E+  EA+K+L  + E     FE++    G     + G+A P+ TI+  
Sbjct: 5   KIAVLAGDGIGPEITQEALKVLKVIEERNDVTFELMPALFGACAYFETGDAFPQATIDIC 64

Query: 58  KEADIILFGAI------TSPKPGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKI 111
            +AD IL G I      +   P + +  +  ++ +R+ ++ YAN RP++      L   +
Sbjct: 65  DQADAILKGPIGLSHEESKKIPVDKQPERGALLPMRRRYNTYANFRPVS------LPKSL 118

Query: 112 ADYEFLN----AKNIDIVIIRENTEDLYVG-RERLENDTAIAERVITRKGSE----RIIR 162
           A +  L      + ID++++RE    LY G +ER  ND  +     T +  E    RI+ 
Sbjct: 119 AHFSPLKPEIIGEGIDLIMVRELVGGLYFGNKERGVNDKGLRYVRETLEYDEEQIRRIMH 178

Query: 163 FAFEYAIKNNRKKVSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIK 221
            AF+ A K  RK +  IHK+NVL ++  L+ EV  E+ K Y ++E  +YLVD+ A  L  
Sbjct: 179 EAFKLASKR-RKLLHNIHKSNVL-MSSVLWNEVMEEVAKDYPDVEVVNYLVDAAATALCL 236

Query: 222 HPEKFDVIVTTNMFGDILSDEASALIGGLGLAPSANIGDDKALFEPVHGSAPDIAGKGIA 281
            P +FDV+V  NMFGDILSD+   ++G LGL PSA IG +KA +EP HGSAPDIAGK IA
Sbjct: 237 KPTQFDVMVMENMFGDILSDQGGGVLGSLGLMPSACIGPEKAYYEPSHGSAPDIAGKNIA 296

Query: 282 NPMASILSIAML----FDYIGEKEKGDLIREAVKYCLINKKVTPDLGGD------LKTKD 331
           NP + I S+AM+    FD   E +    +  A++    +   T DL         + T +
Sbjct: 297 NPYSMIGSVAMMLENSFDMAAEAKN---VWAAMQGVFADGYSTADLSKPGSGVTMISTVE 353

Query: 332 VGDEILNYIRKKLK 345
            GD+++  +R+  K
Sbjct: 354 FGDKVVEKLRQMPK 367


Lambda     K      H
   0.319    0.140    0.397 

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: 333
Number of extensions: 18
Number of successful extensions: 5
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: 347
Length of database: 368
Length adjustment: 29
Effective length of query: 318
Effective length of database: 339
Effective search space:   107802
Effective search space used:   107802
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 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