GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Pontibacter ramchanderi LP43

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_101445722.1 BD749_RS14740 pyridoxal phosphate-dependent aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_002846395.1:WP_101445722.1
          Length = 402

 Score =  137 bits (345), Expect = 5e-37
 Identities = 110/363 (30%), Positives = 175/363 (48%), Gaps = 18/363 (4%)

Query: 32  DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALGIPELRDAIAADYQRRHGITVEP 91
           D++NLS G+P    P+ ++ AA  A+      Y+   G P LR AIA  ++R + +   P
Sbjct: 37  DIINLSFGEPDFQTPQYIKDAAKEAIDEGFTFYTPVPGFPALRQAIADKFKRDNNLDYGP 96

Query: 92  DAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYRNILSALGCEVVEIPCGPQTRFQ 151
           + +V++TG+      A +   + GD V + SP +  Y  I+       V +    +  F+
Sbjct: 97  ENIVVSTGAKQSIANAVMCLVNPGDEVIIFSPYWVSYEEIVKLAEGVPVPLQGRLENDFK 156

Query: 152 PTAQMLAE-IDPPLRGVVVASPANPTGTVIPPEELAAIASWCDA-SDVRLISDEVYHGLV 209
            T + L   I    + V+ +SP NPTG+V   EEL AIA   +    V +I+DE+Y  + 
Sbjct: 157 VTPEQLENAITSNTKVVMYSSPCNPTGSVFDEEELLAIAKVLEKHPQVYIIADEIYEYIN 216

Query: 210 YQGAPQTSCAWQTSRNAVV-VNSFSKYYAMTGWRLGWLLVPTVLRRAVDCLTGNFTICPP 268
           + G   +   +   ++ V+ VN FSK YAMTGWR+G++     +  A + +    T    
Sbjct: 217 FGGKHASMAGFDFIKDRVITVNGFSKGYAMTGWRVGYIAAHKDIATACEKMQSQITSGTC 276

Query: 269 VLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRI-GIDRLAPTDGAFYVYADVS 327
            ++Q AA +A      +  +   A Y   R L+L+ ++ I G     PT GAFY++ DVS
Sbjct: 277 SIAQKAAHAALLGGNESALEMRDA-YRRRRDLVLEIMQGIPGFKTNVPT-GAFYIFPDVS 334

Query: 328 ---------DFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAGPSGDIEEAL 378
                    +  S +L     LL D  VA+  G  F   +    +R S+A     + EAL
Sbjct: 335 YYFGKSYNGNVISSALDLSLYLLTDAHVALVSGEAFGAPQ---CIRFSYATSDDKLIEAL 391

Query: 379 RRI 381
           RRI
Sbjct: 392 RRI 394


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: 363
Number of extensions: 15
Number of successful extensions: 4
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: 402
Length adjustment: 31
Effective length of query: 357
Effective length of database: 371
Effective search space:   132447
Effective search space used:   132447
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 Jul 26 2024. The underlying query database was built on Jul 25 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