GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Clostridium tyrobutyricum FAM22553

Align isocitrate dehydrogenase (NAD+) (EC 1.1.1.41) (characterized)
to candidate WP_039653973.1 PN53_RS14710 isocitrate dehydrogenase (NAD(+))

Query= BRENDA::Q945K7
         (374 letters)



>NCBI__GCF_000816635.1:WP_039653973.1
          Length = 334

 Score =  347 bits (891), Expect = e-100
 Identities = 170/328 (51%), Positives = 235/328 (71%), Gaps = 1/328 (0%)

Query: 47  TLFPGDGIGPEIAESVKKVFTTAGVPIEWEEHYVGTEIDPRTQSFLTWESLESVRRNKVG 106
           TL  GDGIGPE+ ++ +KV   +G  I+WE    G  +     + +    +ES+++NKV 
Sbjct: 6   TLIKGDGIGPEVCKAARKVVDESGAHIDWEVFDAGASVMDEYGTPIPEHIIESIKKNKVA 65

Query: 107 LKGPMATPIGKGHRSLNLTLRKELNLYANVRPCYSLPGYKTRYDDVDLITIRENTEGEYS 166
           LKGP+ TP+GKG RS+N+TLRK LNLYAN+RP  +  G K+RY++VDL+  RENTE  Y+
Sbjct: 66  LKGPVTTPVGKGFRSVNVTLRKSLNLYANIRPIKTYAGVKSRYENVDLVIFRENTEDLYA 125

Query: 167 GLEHQVVRGVVESLKIITRQASLRVAEYAFLYAKTHGRERVSAIHKANIMQKTDGLFLKC 226
           G+EH V   + ES+KII+++AS  +   AF YA  +GR++V+A+HKANIM+ +DGLFL+ 
Sbjct: 126 GIEHMVNDEIAESIKIISKKASANIVRAAFDYAVKNGRKKVTAVHKANIMKLSDGLFLRT 185

Query: 227 CREVAEKYPEITYEEVVIDNCCMMLVKNPALFDVLVMPNLYGDIISDLCAGLVGGLGLTP 286
            +EVA++Y  I +E V++D   M LV NP  +DVLVMPNLYGDI+SD+ +GL+GGLGL P
Sbjct: 186 AQEVAKEYSNIEFESVIVDAMSMKLVLNPENYDVLVMPNLYGDILSDMASGLIGGLGLVP 245

Query: 287 SCNIGEDGVALAEAVHGSAPDIAGKNLANPTALLLSGVMMLRHLKFNEQAEQIHSAIINT 346
             NIGE+  A+ E+ HGSAPDIAG+N ANPTA++LS VMML +L+  E A +I  A+   
Sbjct: 246 GANIGEN-AAVFESAHGSAPDIAGQNKANPTAIILSAVMMLEYLRETEPAHKIEKAVEEV 304

Query: 347 IAEGKYRTADLGGSSTTTEFTKAICDHL 374
           + EGKY T DLGG++TT ++T AI   L
Sbjct: 305 LKEGKYLTGDLGGNATTDQYTDAIVSKL 332


Lambda     K      H
   0.318    0.134    0.389 

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: 352
Number of extensions: 9
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: 374
Length of database: 334
Length adjustment: 29
Effective length of query: 345
Effective length of database: 305
Effective search space:   105225
Effective search space used:   105225
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