GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Ammonifex degensii KC4

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate WP_015739102.1 ADEG_RS05565 homocitrate synthase

Query= BRENDA::Q58787
         (491 letters)



>NCBI__GCF_000024605.1:WP_015739102.1
          Length = 381

 Score =  325 bits (832), Expect = 2e-93
 Identities = 175/370 (47%), Positives = 239/370 (64%), Gaps = 1/370 (0%)

Query: 3   VRIFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKE 62
           +RI DTTLRDGEQT GV  +  +KL IAK LDE+GV  IEAG  +    E E IK I + 
Sbjct: 10  IRIVDTTLRDGEQTAGVVFSNLEKLRIAKMLDEIGVHQIEAGIPVMGGDEAEAIKQICRA 69

Query: 63  GLNAEICSFVRALPVDIDAALECDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALKAVEY 122
           GL A I  + R +  D++A+L C VD+V + + TS IH+++KLR T + V+E  ++AV +
Sbjct: 70  GLKASIMGWNRPVIKDLEASLACGVDAVAISISTSDIHIEHKLRATREWVVEKMVEAVHF 129

Query: 123 AKEHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELFKKIT 182
           AK+HGL V ++AEDA+RSD+ FLI      ++ GADR+  CDTVGVL P  + E  K++ 
Sbjct: 130 AKKHGLYVSVNAEDASRSDMEFLIAFARAAKEAGADRLRYCDTVGVLDPFTTYENIKRLV 189

Query: 183 ENVNLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEVVAALKILY 242
             V LP+ +H HNDFGMATAN  + VL GA    VTV G+GERAGNA+LEEVV ALK ++
Sbjct: 190 SEVGLPIEMHTHNDFGMATANALAGVLAGADWIGVTVCGLGERAGNAALEEVVMALKHIF 249

Query: 243 GYDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLIKNTETYEPIK 302
           G D   K E   E++  VS      +P  K IVG N FAHE+GIH DG +KN +TYE  +
Sbjct: 250 GVDLGFKTELFREIAEYVSHAAHRELPAWKPIVGSNMFAHESGIHADGALKNPKTYEAFQ 309

Query: 303 PEMVGNRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFG-DLGKYISDADL 361
           PE VG  R+I++GKHSG  AL+ K    GI++S  +   +   V++    L + + D +L
Sbjct: 310 PEEVGLTRQIVIGKHSGTAALRAKFAEYGISLSKHEAELLLPEVRKAAVSLKRPLFDKEL 369

Query: 362 LAIVREVTGK 371
           ++I  E+ G+
Sbjct: 370 VSIYEELFGR 379


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: 478
Number of extensions: 15
Number of successful extensions: 1
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: 381
Length adjustment: 32
Effective length of query: 459
Effective length of database: 349
Effective search space:   160191
Effective search space used:   160191
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 10 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