GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Sinorhizobium medicae WSM419

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate YP_001325872.1 Smed_0178 class I and II aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_000017145.1:YP_001325872.1
          Length = 396

 Score =  142 bits (357), Expect = 2e-38
 Identities = 107/366 (29%), Positives = 170/366 (46%), Gaps = 11/366 (3%)

Query: 23  AAERQRTHGDLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQ 82
           A + + +  D++ L+ G+P       +      A++  +  YS   G P +  A+   Y+
Sbjct: 24  ARQLKASGADIIELTIGEPDLPPDPALLEECQRAMNAGRYRYSNGRGEPAVVAALTEKYR 83

Query: 83  RRH-GITVEPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVE 141
           RR  G+T E   ++   G+            +AGD V +  P Y  Y  ++ + G   V 
Sbjct: 84  RRRSGVTKEN--ILCFPGTQTALFAVMFGLAEAGDGVLVGDPLYATYEGVIRSTGAHPVF 141

Query: 142 IPCGPQTRFQPTAQMLAE-IDPPLRGVVVASPANPTGTVIPPEELAAIASWCDASDVRLI 200
           +P  PQ  F   A+ L + + P  R +++ +P NPTG V+ PEE+AAI +     D+ ++
Sbjct: 142 VPLNPQHGFHMQAEDLEKAVTPECRVLLLNTPHNPTGAVLTPEEIAAIGAVARRHDLWIV 201

Query: 201 SDEVYHGLVYQGA-PQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWLLVPTVLRRAVDCL 259
            DEVY  LV+  A          +   VVV+S SK +A TG+R GW + P      +  +
Sbjct: 202 CDEVYEELVFDAAFASPFDNPDLAERTVVVSSISKSHAATGFRSGWAVGPAEFTERLLPI 261

Query: 260 TGNFTI-CPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIGIDRLAPTDG 318
           +        P ++ + A +      TA       SY+    L +DGL  +    + P + 
Sbjct: 262 SETMLFGQQPFIADMTAYALTHEIGTARQ--MRESYSHRARLTIDGLAGVPGVSVLPPEA 319

Query: 319 AFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDF-DTARGGSFVRISFAGPSGDIEEA 377
             +   DVS  +    AF   LL + GVA+ PG  F DTAR  +F+R+S   P   IEEA
Sbjct: 320 GMFALIDVSGTSLSGEAFAWALLEEEGVAVMPGSSFGDTAR--NFLRVSLTVPDDVIEEA 377

Query: 378 LRRIGS 383
            RRI +
Sbjct: 378 CRRIAA 383


Lambda     K      H
   0.321    0.136    0.416 

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: 401
Number of extensions: 24
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: 388
Length of database: 396
Length adjustment: 31
Effective length of query: 357
Effective length of database: 365
Effective search space:   130305
Effective search space used:   130305
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 (21.9 bits)
S2: 50 (23.9 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