GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Ammonifex degensii KC4

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; Beta-IPM dehydrogenase; IMDH; EC 1.1.1.85 (characterized)
to candidate WP_015739918.1 ADEG_RS09915 3-isopropylmalate dehydrogenase

Query= SwissProt::P9WKK9
         (336 letters)



>NCBI__GCF_000024605.1:WP_015739918.1
          Length = 353

 Score =  324 bits (831), Expect = 2e-93
 Identities = 182/349 (52%), Positives = 231/349 (66%), Gaps = 16/349 (4%)

Query: 2   KLAIIAGDGIGPEVTAEAVKVLDAVVP----GVQKTSYDLGARRFHATGEVLPDSVVAEL 57
           ++A+I GDG GPE   E +KVL+AV        +   YD G  R+  TGE LPDS + EL
Sbjct: 4   RIAVIPGDGTGPEQVREGLKVLEAVAQLEGFKYETVVYDFGGERYLRTGETLPDSAIEEL 63

Query: 58  RNHDAILLGAIGDPSVPSGVLERGLLLRLRFELDHHINLRPARLYPGVASPLS--GNPGI 115
           +   AI LGAIG P V  G+LE+G+LLRLRFELD +INLRP +LYPGV +PL   G   I
Sbjct: 64  KQFHAIYLGAIGHPDVKPGILEKGILLRLRFELDQYINLRPVKLYPGVETPLKDKGPEDI 123

Query: 116 DFVVVREGTEGPYTGNGGAIRVGTPNEVATEVSVNTAFGVRRVVADAFE--RARRRRKHL 173
           DFVVVRE TEG Y G GG +R GT +EVA ++S+NT  GV R V  AFE  R R ++K +
Sbjct: 124 DFVVVRENTEGLYCGAGGFLRRGTKDEVALQISINTYKGVERCVRYAFEYCRKRNKKKKV 183

Query: 174 TLVHKTNVLTFAGGLWLRTVDEVGECYPDVEVAYQHVDAATIHMITDPGRFDVIVTDNLF 233
           TL  KTNVLT+A  LW R    VGE YPD+   Y HVDA  + M+ +P  FDVIVTDN+F
Sbjct: 184 TLCGKTNVLTYAFDLWERVFHAVGEEYPDITRDYAHVDAICMWMVKNPEWFDVIVTDNMF 243

Query: 234 GDIITDLAAAVCGGIGLAASGNIDATRANPSMFEPVHGSAPDIAGQGIADPTAAIMSVAL 293
           GDIITDL A + GG+G+AA  NI+      SMFEP+ GSAP  AG+   +P AAI+++A+
Sbjct: 244 GDIITDLGAIIQGGLGIAAGANINP--QGVSMFEPIGGSAPKYAGKNQINPLAAILALAM 301

Query: 294 LLSHLGEHDAAARVDRAVE----AHLATRGSERL--ATSDVGERIAAAL 336
           LL HLGE  AAAR++RAV+     HL +  + R+   TS+VG+ +   L
Sbjct: 302 LLEHLGEERAAARIERAVQEVCSKHLKSLAAGRMGYTTSEVGDLVVRYL 350


Lambda     K      H
   0.319    0.137    0.398 

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: 337
Number of extensions: 18
Number of successful extensions: 6
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: 336
Length of database: 353
Length adjustment: 29
Effective length of query: 307
Effective length of database: 324
Effective search space:    99468
Effective search space used:    99468
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