GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Herbaspirillum seropedicae SmR1

Align Predicted argE by GapMind curators (no experimental data)
to candidate HSERO_RS15925 HSERO_RS15925 amidohydrolase

Query= predicted:W3Y6L2
         (394 letters)



>FitnessBrowser__HerbieS:HSERO_RS15925
          Length = 399

 Score =  239 bits (609), Expect = 1e-67
 Identities = 125/366 (34%), Positives = 205/366 (56%), Gaps = 4/366 (1%)

Query: 16  KEQVVAWRRHIHSHPELSGEEKETSAFIQSVLTDLGIPFKADVYKYAVIGEIKGAFDGPV 75
           ++++ A RRH+H HPELS EE +T+A +   L   G      +    ++  ++       
Sbjct: 19  QDEITAIRRHLHQHPELSFEEVDTAALVAQRLEQWGYAVTRHIGGNGLVATLRVGSSARS 78

Query: 76  VGLRADMDALPITEVTGLPFTSENPGVMHACGHDSHMAILLGAAAILQSVKDQLHGTVKL 135
           +GLRADMDALPI E TGL + S  PG MHACGHD H A+LLGAA  L   + +  GT+ L
Sbjct: 79  IGLRADMDALPIQEETGLDWASVKPGAMHACGHDGHTAMLLGAARHLARTR-RFDGTLNL 137

Query: 136 VIQPAEEEALIKGAQGIVDSGVLD--DVDEIYGLHVWPQLPVGTVGLKKGNLMAASDRFL 193
           + QPAEE     GAQ ++  G+ +    + ++G+H  P +  GT   + G  MAA D   
Sbjct: 138 IFQPAEEAGFDSGAQKMLADGLFERFPCEAVFGIHNHPGVEAGTFMFRSGPFMAACDTVK 197

Query: 194 VHIKGKATHGAEPHNGIDAIVAAANWIVNVESMVARETNPMDNLVCTIGVFNSGDRYNVG 253
           + I G+ +H A PH  +D +V AA+ ++ ++++V+R  +PMD+ V T+G  ++G   NV 
Sbjct: 198 IRITGRGSHAARPHLSVDPVVVAASLVMALQTVVSRNIDPMDSAVVTVGSLHAGKASNVI 257

Query: 254 SGDAYLEGTCRTYDPAKRDYIERRLGESLKALDMMFGTTSTLEYRRGHGATINDADAIDY 313
              A +E + R++ P  R+ +E+R+   +      +G  + ++Y RG+   +N     D+
Sbjct: 258 PEFATMELSVRSFKPEVRELLEQRIRALVSTHAQSYGAQAEIDYLRGYPVLVNSDAETDF 317

Query: 314 VTHIVKTYLGKDAVVHPEFPSMAAEDFSAYLNKIKGAFLWLGTGFEGNPALHNAAFTIDE 373
              + +  +G + V+ P  P   +EDF+ +L +  G FL +G G +G P LHNA +  ++
Sbjct: 318 ARSVAEELVGPEKVIAPFGPIAGSEDFAYFLRQRPGCFLRVGNG-QGKPMLHNAGYDFND 376

Query: 374 SILEPG 379
           + +  G
Sbjct: 377 ANIPIG 382


Lambda     K      H
   0.318    0.136    0.401 

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: 399
Number of extensions: 13
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: 394
Length of database: 399
Length adjustment: 31
Effective length of query: 363
Effective length of database: 368
Effective search space:   133584
Effective search space used:   133584
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: 50 (23.9 bits)

This GapMind analysis is from Jul 25 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