GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Methanosarcina mazei Go1

Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_011032593.1 MM_RS03355 3-isopropylmalate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000007065.1:WP_011032593.1
          Length = 330

 Score =  278 bits (712), Expect = 1e-79
 Identities = 163/337 (48%), Positives = 218/337 (64%), Gaps = 17/337 (5%)

Query: 3   KICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDCD 62
           ++ VIEGDGIG+EV+PA ++VL+A GL FE V  E G   ++RTG A+ EE +E    C+
Sbjct: 2   RLAVIEGDGIGREVIPAAVEVLDAFGLEFEKVPLEIGYARWERTGTAMSEEDMEIIKSCN 61

Query: 63  AVLFGAAGETAAD-----VIVKLRHILDTYANIRPVKAYKGVKCL--RPDIDYVIVRENT 115
           AVLFGA   T  D     V++ +R  LD YAN+RPVK   GV  +  R D D++IVRENT
Sbjct: 62  AVLFGAV-TTVPDPGYKSVLLTIRKELDLYANVRPVKPLSGVVGVSGRSDFDFIIVRENT 120

Query: 116 EGLYKGIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVLK 175
           EGLY GIE EI   ++   RVIT K  ERI  +A  LA++R      GK+T  HK+NVLK
Sbjct: 121 EGLYSGIE-EIGHDLSWTKRVITRKGSERISEYACELAKKRS-----GKLTIVHKSNVLK 174

Query: 176 LTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAG 235
            +D LF  +  + A  Y  ++  D  +D+M   +I  P+ +DVVVT+NLFGDILSD  A 
Sbjct: 175 -SDKLFLDVCRETASSYG-VEYGDMLVDSMAYSLIMHPEKYDVVVTTNLFGDILSDMCAA 232

Query: 236 TVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADK 295
            VG LGL PSANIG ++  FEPVHGSAPDIAGK I+NP A IL   ++L ++G+ EA   
Sbjct: 233 LVGSLGLVPSANIGKKYAFFEPVHGSAPDIAGKGISNPLAAILCVKMLLEWMGKPEAR-L 291

Query: 296 VEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRVRE 332
           ++ A+ ++L   + TPDLGG  +T E+   VAK + +
Sbjct: 292 IDAAIADLLQKKIITPDLGGRASTAEVGNAVAKYIMQ 328


Lambda     K      H
   0.318    0.138    0.390 

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: 302
Number of extensions: 13
Number of successful extensions: 7
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: 333
Length of database: 330
Length adjustment: 28
Effective length of query: 305
Effective length of database: 302
Effective search space:    92110
Effective search space used:    92110
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 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