GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Pedobacter sp. GW460-11-11-14-LB5

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate CA265_RS15855 CA265_RS15855 2-isopropylmalate synthase

Query= BRENDA::Q58787
         (491 letters)



>FitnessBrowser__Pedo557:CA265_RS15855
          Length = 386

 Score =  283 bits (725), Expect = 6e-81
 Identities = 166/374 (44%), Positives = 222/374 (59%), Gaps = 11/374 (2%)

Query: 3   VRIFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKE 62
           V IFDTTLRDGEQ PG  L  N K+EIAK L+ LGVDVIEAG  ++S G+   +  ++K 
Sbjct: 8   VYIFDTTLRDGEQVPGCQLDTNQKVEIAKSLELLGVDVIEAGFPVSSPGDFNSVIELSKA 67

Query: 63  GLNAEICSFVRALPVDIDAALE----CDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALK 118
             N  IC+  RA   DID A +         +H  + +S  H+K+K   T +E+LE A++
Sbjct: 68  VTNPIICALTRANKNDIDVAADALRYAKRPRIHTGIGSSDFHIKHKFNSTREEILERAVE 127

Query: 119 AVEYAKEHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELF 178
           AV Y+K+    VE  AEDA R+D+ FL K+       GA  V + DT G   P +     
Sbjct: 128 AVRYSKKFVEDVEFYAEDAGRADIEFLAKMVEAVIAAGATVVNIPDTNGYCLPDQYGSKI 187

Query: 179 KKITENV----NLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEV 234
             + ENV       +SVHCHND G+ATAN+ + +  GA Q   T+NGIGERAGN S+EEV
Sbjct: 188 LFLKENVKNIDKAIISVHCHNDLGLATANSIAGLQNGARQVECTINGIGERAGNTSMEEV 247

Query: 235 VAALKI--LYGYDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLI 292
           V  LK   + G +T+I   + YE+S +V   M +PV PNKAIVG NAF+H +GIH DG +
Sbjct: 248 VMILKTHKILGLNTQIDATRFYEMSHMVRNQMNMPVQPNKAIVGGNAFSHSSGIHQDGFL 307

Query: 293 KNTETYEPIKPEMVG-NRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFGD 351
           KN E YE IKPE VG     I+L   SGR ALK+ LD +G  +  + L+ +Y++     D
Sbjct: 308 KNRENYEIIKPEDVGFPDATIVLTARSGRHALKHHLDRLGHKLEKDHLDIVYKQFLVLAD 367

Query: 352 LGKYISDADLLAIV 365
             + I+D DL  +V
Sbjct: 368 SKQGINDQDLNQLV 381


Lambda     K      H
   0.316    0.136    0.373 

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: 481
Number of extensions: 31
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: 491
Length of database: 386
Length adjustment: 32
Effective length of query: 459
Effective length of database: 354
Effective search space:   162486
Effective search space used:   162486
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 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