GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Rhodospirillum rubrum ATCC 11170

Align Predicted argE by GapMind curators (no experimental data)
to candidate WP_011389566.1 RRU_RS09420 M20 aminoacylase family protein

Query= predicted:W3Y6L2
         (394 letters)



>NCBI__GCF_000013085.1:WP_011389566.1
          Length = 388

 Score =  238 bits (608), Expect = 2e-67
 Identities = 132/377 (35%), Positives = 213/377 (56%), Gaps = 10/377 (2%)

Query: 19  VVAWRRHIHSHPELSGEEKETSAFIQSVLTDLGIPFKAD-VYKYAVIGEIKGAFDGPVVG 77
           ++ WR  IH HPEL  +E  T+A +  +L   G     + +    V+G ++   DGP++G
Sbjct: 14  MIDWRHDIHRHPELGYQETRTAAKVAGLLRGFGCDAVVEQIGGTGVVGVLRQG-DGPMIG 72

Query: 78  LRADMDALPITEVTGLPFTSENPGVMHACGHDSHMAILLGAAAILQSVKDQLHGTVKLVI 137
           LRADMDALPI E       S +PGVMHACGHD H A+LLGAA  L + + +  G+V  + 
Sbjct: 73  LRADMDALPIPERNDFDHQSVHPGVMHACGHDGHTAMLLGAARHLAATR-RFQGSVVFIF 131

Query: 138 QPAEEEALIKGAQGIVDSGVLD--DVDEIYGLHVWPQLPVGTVGLKKGNLMAASDRFLVH 195
           QPAEE   + GA+ +++ G+ +   V+ +YGLH  P LP G++ +  G  +AA+D+ ++ 
Sbjct: 132 QPAEEG--LAGARAMIEDGLFERWPVEAVYGLHNLPGLPAGSISVSPGPQLAAADKLVIE 189

Query: 196 IKGKATHGAEPHNGIDAIVAAANWIVNVESMVARETNPMDNLVCTIGVFNSGDRYNVGSG 255
           I G+  H A P    D ++A A  +  ++ +V+R  +P +  V ++  FN+G+ +NV   
Sbjct: 190 ITGRGAHAAAPELARDPVLAGAAAVQALQQIVSRNVSPAETAVVSVTCFNAGETFNVLPD 249

Query: 256 DAYLEGTCRTYDPAKRDYIERRLGESLKALDMMFGTTSTLEYRRGHGATINDADAIDYVT 315
            A L+GT R +     D +  R+ + L+ + +    + TL+ +RG+ AT+N A   D+  
Sbjct: 250 GATLKGTVRYFSSETGDLVRNRIAQVLEGIALAHDVSITLDLQRGYPATVNSAPQADFAR 309

Query: 316 HIVKTYLGKDAVVHPEFPSMAAEDFSAYLNKIKGAFLWLGTGFEGNPALHNAAFTIDESI 375
            + +  LG+D +  P+ P M AEDFS  L    GAF ++G G   +P+LHN  +  +++I
Sbjct: 310 GVARALLGED-LAPPQEPRMIAEDFSLMLQVKPGAFGFIGNG--QSPSLHNPRYEFNDAI 366

Query: 376 LEPGITMMAGIAAELLQ 392
           L  G      +A   L+
Sbjct: 367 LPIGAAYFCALAETALR 383


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: 395
Number of extensions: 16
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: 388
Length adjustment: 31
Effective length of query: 363
Effective length of database: 357
Effective search space:   129591
Effective search space used:   129591
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