GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Dyella japonica UNC79MFTsu3.2

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; EC 1.1.1.85; Beta-IPM dehydrogenase (uncharacterized)
to candidate N515DRAFT_1138 N515DRAFT_1138 isocitrate dehydrogenase (NAD+)

Query= curated2:O29627
         (326 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1138
          Length = 338

 Score =  303 bits (776), Expect = 4e-87
 Identities = 162/329 (49%), Positives = 214/329 (65%), Gaps = 9/329 (2%)

Query: 2   KKIVVIPGDGIGKEVMEAAMLILEKLDLPFEYSYYDAGDEALEKYGKALPDETLEACRKS 61
           K I VIPGDGIG E+M+A + +L+ LD    Y + DAG  ALEK+G  LP +TL+A  + 
Sbjct: 3   KTIAVIPGDGIGPEIMKATLRVLDALDCGLSYEFVDAGMVALEKHGDLLPKDTLDAIARH 62

Query: 62  DAVLFGAA----GETAADVIVRLRRELGTFANVRPAKAIEGIECLYPGLDIVVVRENTEC 117
              L G      G     + V LRR    +ANVRPA +  G +  +  +DI+ VRENTE 
Sbjct: 63  TIALKGPLTTPIGGGFTSINVTLRRHFDLYANVRPAISFPGTKARFENIDIITVRENTEG 122

Query: 118 LYMGFEFGF---GDVTEAIRVITREASERIARYAFELAKREGRKKVTALHKANVMKKTCG 174
            Y+         G+V  ++   TR+ S RI +YAFE+A+++GRKK+TA+HKAN+MK + G
Sbjct: 123 AYLSEGQTLSEDGEVATSMVRNTRKGSTRIVKYAFEMARQKGRKKITAVHKANIMKTSSG 182

Query: 175 LFRDVCREVAKDYPEIQYNDYYIDAACMYLVMDPFRFDVIVTTNMFGDIVSDLAAGLVGG 234
           LF +V REVAK+YP+I++N+  +D  CM LVM P +FDVIVTTN+FGDI+SDL AGLVGG
Sbjct: 183 LFLNVAREVAKEYPDIEFNEMIVDNTCMQLVMKPEQFDVIVTTNLFGDILSDLCAGLVGG 242

Query: 235 LGLAPSANVGERTAIFEPVHGAAFDIAGKGIANPTAMILTACMMLRHFGYVEEAKKVEEA 294
           LGLAP  N+G   AIFE VHG+A DIAGKGIANP A++L A  ML H G  ++  KV  A
Sbjct: 243 LGLAPGDNIGAGAAIFEAVHGSAPDIAGKGIANPCALLLAAADMLDHLGMADKGNKVRAA 302

Query: 295 VEKTIKEGKK--TPDLGGNLKTMEFANEV 321
           +  T+   +   TPDLGG   T  F + +
Sbjct: 303 IRDTLTNDRDAVTPDLGGKGNTDSFGDAI 331


Lambda     K      H
   0.321    0.139    0.399 

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: 316
Number of extensions: 11
Number of successful extensions: 4
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: 326
Length of database: 338
Length adjustment: 28
Effective length of query: 298
Effective length of database: 310
Effective search space:    92380
Effective search space used:    92380
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: 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