GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Phyllobacterium endophyticum PEPV15

Align isocitrate dehydrogenase (NAD+) (EC 1.1.1.41) (characterized)
to candidate WP_106714781.1 CU100_RS01435 3-isopropylmalate dehydrogenase

Query= BRENDA::P93032
         (367 letters)



>NCBI__GCF_003010935.1:WP_106714781.1
          Length = 370

 Score =  116 bits (291), Expect = 8e-31
 Identities = 111/373 (29%), Positives = 181/373 (48%), Gaps = 59/373 (15%)

Query: 38  RPVTLIPGDGVGPLVTNAVQQVMEAMHAPVYFE-----------PFEVHGDMKSLPEGLL 86
           + + L+PGDG+GP     V++++  M++ +  E            ++ HG   ++ E  +
Sbjct: 4   KKLLLLPGDGIGPEAMAEVRKIIGYMNSELKSEFVLDEGLVGGSAYDAHG--AAISEADM 61

Query: 87  ESIKKNKVCLKGGLKTPVGGGV------SSLNVNLRKELDLFASLVNCFNLPGLASRH-- 138
                    L G +  P    V       +  + LRK+++LFA+L      P LA     
Sbjct: 62  AKALAADAVLFGAVGGPKWDSVPYDVRPEAGLLRLRKDMELFANLRPAICYPALADSSSL 121

Query: 139 -----ENVDIVVIRENTEGEYAGLEHEVVP-------GVVESLKVITKFCSERIAKYAFE 186
                E +DI+++RE T G Y G   E+         G+    +V   +  ERI+  AFE
Sbjct: 122 KKEIVEGLDILIVRELTGGVYFGEPKEIRDLGNGQKRGI--DTQVYDTYEIERISGVAFE 179

Query: 187 YAYLNNRKKVTAVHKANIMKLADGLFLESCQEVAK-KYPSIAYNEIIVDNCCMQLVARPE 245
            A     K VT++ K N+MK +  L+ E      K KY  +    ++ D   MQLV  P+
Sbjct: 180 LARTRGNK-VTSMEKRNVMK-SGVLWNEVVTATHKTKYSDVKLEHMLADAGGMQLVRWPK 237

Query: 246 QFDVMVTPNLYGNLVANTAAGIAGGTGVMPGGNVGA-------EYAVFE--QGASAGNVG 296
           QFDV+VT NL+G+++++ AA + G  G++P  ++GA         A++E   G++    G
Sbjct: 238 QFDVIVTDNLFGDMLSDIAAMLTGSLGMLPSASLGAPDAKTGKRKALYEPVHGSAPDIAG 297

Query: 297 KDTTEEQKNANPVALLLSSAMMLRH-LQFPSFADRLETAVKRVIAEGNCRTEDLGGNSTT 355
             T      ANP+A++ S AM LR+     + ADRLE+AV  V+ +G  RT D+     T
Sbjct: 298 TGT------ANPIAMIASFAMCLRYSFNMIAEADRLESAVAGVLDDG-LRTADIMAEGKT 350

Query: 356 Q----EVVDAVIA 364
           +    E+ DA++A
Sbjct: 351 RIGTAEMGDAILA 363


Lambda     K      H
   0.316    0.134    0.381 

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: 280
Number of extensions: 14
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: 367
Length of database: 370
Length adjustment: 30
Effective length of query: 337
Effective length of database: 340
Effective search space:   114580
Effective search space used:   114580
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 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 26 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