GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Leptospirillum ferrooxidans C2-3

Align isocitrate dehydrogenase (NAD+) (EC 1.1.1.41) (characterized)
to candidate WP_014448976.1 LFE_RS03940 isocitrate/isopropylmalate dehydrogenase family protein

Query= BRENDA::Q945K7
         (374 letters)



>NCBI__GCF_000284315.1:WP_014448976.1
          Length = 336

 Score =  336 bits (862), Expect = 5e-97
 Identities = 160/324 (49%), Positives = 226/324 (69%), Gaps = 1/324 (0%)

Query: 47  TLFPGDGIGPEIAESVKKVFTTAGVPIEWEEHYVGTEIDPRTQSFLTWESLESVRRNKVG 106
           T+ PG+G GPEI E+V++V   +GV I WE   +G +      + L  ++++S+ +NK+ 
Sbjct: 7   TMLPGEGTGPEICEAVRRVIDHSGVDITWEYEEIGLDCLKEHGTLLPEKTIKSIAKNKIA 66

Query: 107 LKGPMATPIGKGHRSLNLTLRKELNLYANVRPCYSLPGYKTRYDDVDLITIRENTEGEYS 166
           +KGP  TP+G GH+S N+TLRK  +LYANVRP   +P  K  +D +D+++ RENTE  Y+
Sbjct: 67  IKGPTTTPVGTGHKSANVTLRKMFDLYANVRPAKLIPVLKRPWDKIDILSFRENTEDSYA 126

Query: 167 GLEHQVVRGVVESLKIITRQASLRVAEYAFLYAKTHGRERVSAIHKANIMQKTDGLFLKC 226
            +EH V   V + LK+IT   S+R+AE+AF +A+ + R+++  +HKANIM+ TDGLFL+ 
Sbjct: 127 AIEHMVSDEVAQCLKVITWPGSIRIAEFAFKWARANNRKKMQCVHKANIMKMTDGLFLEA 186

Query: 227 CREVAEKYPEITYEEVVIDNCCMMLVKNPALFDVLVMPNLYGDIISDLCAGLVGGLGLTP 286
            REVA+ YP+I  E++++DNC M LV+NP  FD LV+PNLYGDI+SDLCAGLVGGLG  P
Sbjct: 187 FREVAKNYPDIVAEDIIVDNCSMQLVRNPGQFDCLVLPNLYGDILSDLCAGLVGGLGFAP 246

Query: 287 SCNIGEDGVALAEAVHGSAPDIAGKNLANPTALLLSGVMMLRHLKFNEQAEQIHSAIINT 346
             NIG D  ++ EAVHGSAP  AG    NP+A+LLSGVMML+ L  +E A +I   +   
Sbjct: 247 GANIG-DNCSIFEAVHGSAPKYAGMKKVNPSAVLLSGVMMLKWLNEHEAATRIEKGVDKV 305

Query: 347 IAEGKYRTADLGGSSTTTEFTKAI 370
           +AE K+ T D GG+++T E+  AI
Sbjct: 306 LAEAKHLTYDAGGTASTDEYADAI 329


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: 405
Number of extensions: 12
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: 336
Length adjustment: 29
Effective length of query: 345
Effective length of database: 307
Effective search space:   105915
Effective search space used:   105915
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.

Links

Downloads

Related tools

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