GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Phyllobacterium brassicacearum STM 196

Align Predicted argE by GapMind curators (no experimental data)
to candidate WP_106711061.1 CU102_RS09815 amidohydrolase

Query= predicted:W3Y6L2
         (394 letters)



>NCBI__GCF_003010955.1:WP_106711061.1
          Length = 387

 Score =  268 bits (686), Expect = 2e-76
 Identities = 147/384 (38%), Positives = 228/384 (59%), Gaps = 9/384 (2%)

Query: 12  ASQYKEQVVAWRRHIHSHPELSGEEKETSAFIQSVLTDLGIP-FKADVYKYAVIGEIKGA 70
           A + ++ V  WR H+H +PE+  +  +TSAF+   L + G    +  + +  V+G ++G 
Sbjct: 7   AHEMQQHVAEWRHHLHENPEILYDVHQTSAFVAEKLREFGCDTIETGIGQTGVVGLVRGR 66

Query: 71  F-DGPVVGLRADMDALPITEVTGLPFTSENPGVMHACGHDSHMAILLGAAAILQSVKDQL 129
             +GPV+G RADMDALPITE +G P+ S+  G MHACGHD H A+LLGAA  L   ++  
Sbjct: 67  HGEGPVIGFRADMDALPITEASGKPWASKTLGKMHACGHDGHTAMLLGAAQYLAETRN-F 125

Query: 130 HGTVKLVIQPAEEEALIKGAQGIVDSGVLDD--VDEIYGLHVWPQLPVGTVGLKKGNLMA 187
            GT+ L+ QPAEE     GA+ ++D G++D   + E+YG+H  P LPVG    +KG++MA
Sbjct: 126 RGTIVLIFQPAEEGGA--GARAMIDDGLMDRFAIGEVYGMHNAPGLPVGQFATRKGSIMA 183

Query: 188 ASDRFLVHIKGKATHGAEPHNGIDAIVAAANWIVNVESMVARETNPMDNLVCTIGVFNSG 247
           A++ F + + G++ H A+PH  ID +V +A+ I+ ++S+V+RET+P+  LV ++   N G
Sbjct: 184 ATNEFEITVTGRSGHAAKPHTAIDPVVISAHIILALQSIVSRETDPLKALVVSVTQLNGG 243

Query: 248 DRYNVGSGDAYLEGTCRTYDPAKRDYIERRLGESLKALDMMFGTTSTLEYRRGHGATIND 307
           D  NV      L GT RT  P  R++ ++RL E +++   +FG  + + Y +G+  T N 
Sbjct: 244 DATNVIPDVIKLGGTVRTLVPEIREFAQKRLTEIVESTAAVFGGKAEVVYHQGYPVTFNH 303

Query: 308 ADAIDYVTHIVKTYLGKDAVVHPEFPSMAAEDFSAYLNKIKGAFLWLGTGFEGNPALHNA 367
               D+   I +T +G+ AV     P M AEDFS  L    GAF++LG G    P LHN+
Sbjct: 304 DRETDFAIGIAQTIVGEAAVNTTMPPVMGAEDFSYMLESRPGAFVFLGNG--DTPGLHNS 361

Query: 368 AFTIDESILEPGITMMAGIAAELL 391
           A+  ++  +  GI+    +A   L
Sbjct: 362 AYDFNDDAIPYGISYWVSLAETAL 385


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: 400
Number of extensions: 17
Number of successful extensions: 5
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: 387
Length adjustment: 31
Effective length of query: 363
Effective length of database: 356
Effective search space:   129228
Effective search space used:   129228
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 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