GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Klebsiella michiganensis M5al

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate BWI76_RS18860 BWI76_RS18860 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>FitnessBrowser__Koxy:BWI76_RS18860
          Length = 380

 Score =  232 bits (591), Expect = 2e-65
 Identities = 140/378 (37%), Positives = 204/378 (53%), Gaps = 3/378 (0%)

Query: 12  DEVRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIA 71
           + V I DTTLRDGEQ+PGVA    EK+ IA  L   G+  +E G  A  + E+  I+ + 
Sbjct: 2   ERVLINDTTLRDGEQSPGVAFRTSEKVAIAEALYAAGITAMEVGTPAMGDEEIARIQLVR 61

Query: 72  REELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVV 131
           R+  DA + +  RM   ++  + +   D V I +P S+   + KLR     +LER    +
Sbjct: 62  RQLPDATLMTWCRMNALEIRQSADLGIDWVDISIPASDKLRQYKLREPLAVLLERLAMFI 121

Query: 132 EYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKK 191
             A   GL V I  ED +R   + L  + +   +  A RL Y DTVG++ P      +  
Sbjct: 122 HLAHTLGLKVCIGCEDASRASGQTLRAIAEVAQQCAAARLRYADTVGLLDPFTTAAQISA 181

Query: 192 LRERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVL 251
           LR+    ++   +H H+D GMATANT+AAV AGA  V+ TV G+GERAGNAALE V + L
Sbjct: 182 LRDVWSGEI--EMHAHNDLGMATANTLAAVSAGATSVNTTVLGLGERAGNAALETVALGL 239

Query: 252 EELYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTY 311
           E   GV+TG+    L  L + V       + P + +VGE  FTHESG+H   +L+D  +Y
Sbjct: 240 ERCLGVETGVHFSALPALCQRVAEAAQRAIDPQQPLVGELVFTHESGVHVAALLRDSESY 299

Query: 312 EPIPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKRI-T 370
           + I P  +G   R VLGKH G   +     QMG  ++  Q+ ++L  ++R  +  KR   
Sbjct: 300 QSIAPSLMGRSYRLVLGKHSGRQAVNGVFDQMGYHLNAAQINQLLPAIRRFAENWKRSPK 359

Query: 371 EADLRAIAEDVLGRPAER 388
           + +L AI +++ G  A R
Sbjct: 360 DYELVAIYDELCGESALR 377


Lambda     K      H
   0.315    0.134    0.367 

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: 407
Number of extensions: 19
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: 509
Length of database: 380
Length adjustment: 32
Effective length of query: 477
Effective length of database: 348
Effective search space:   165996
Effective search space used:   165996
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.

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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