GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Clostridium kluyveri DSM 555

Align Predicted argE by GapMind curators (no experimental data)
to candidate WP_012101872.1 CKL_RS07285 M20 family metallopeptidase

Query= predicted:W3Y6L2
         (394 letters)



>NCBI__GCF_000016505.1:WP_012101872.1
          Length = 390

 Score =  226 bits (577), Expect = 7e-64
 Identities = 137/386 (35%), Positives = 207/386 (53%), Gaps = 9/386 (2%)

Query: 12  ASQYKEQVVAWRRHIHSHPELSGEEKETSAFIQSVLTDLGIPFKADVYKYAVIGEIKGAF 71
           A   K++++  RR +H HPEL  EE+ TS  I+  L  +GI +  +     V G I+G  
Sbjct: 9   AQSIKKELIDIRRDLHRHPELGYEEERTSFKIKEFLKKIGIEYM-ETAGTGVCGIIRGK- 66

Query: 72  DGPVVGLRADMDALPITEVTGLPFTSENPGVMHACGHDSHMAILLGAAAILQSVKDQLHG 131
               +G+RAD+DALP+ +     ++S+  G MHACGHD+H  ILLG A +L SVKD+L G
Sbjct: 67  GNKTIGIRADIDALPLEDHKNCSYSSKVKGKMHACGHDAHTTILLGTAKVLNSVKDELKG 126

Query: 132 TVKLVIQPAEEEALIKGAQGIVDSGVLDD--VDEIYGLHVWPQLPVGTVGLKKGNLMAAS 189
           TVKL  +PAEE     GA+ +V  G L++  VD + GLHV   + VG +G+K G + AAS
Sbjct: 127 TVKLFFEPAEETT--GGAKLMVKEGALENPRVDRVIGLHVDENIEVGNIGVKLGVVNAAS 184

Query: 190 DRFLVHIKGKATHGAEPHNGIDAIVAAANWIVNVESMVARETNPMDNLVCTIGVFNSGDR 249
           + F + IKG   HGA PH G+D IV +++ I+ ++ +V+RE  P D  V T+G  + G  
Sbjct: 185 NPFTIKIKGVGAHGARPHMGVDPIVISSHVILALQQIVSRELPPTDAAVITVGSIHGGTA 244

Query: 250 YNVGSGDAYLEGTCRTYDPAKRDYIERRLGESLKALDMMFGTTSTLEYRRGHGATINDAD 309
            N+   +  + GT RT     R+Y++ RL E    +         ++    +    ND D
Sbjct: 245 QNIIPEEVVIAGTMRTMRTEHREYVKERLREITFGVVNSMRGKYEIDIEESYPCLYNDDD 304

Query: 310 AIDYVTHIVKTYLGKDAVVHPEFPSMAAEDFSAYLNKIKGAFLWLGTGFEGNPAL---HN 366
            I  +       +G++ V   E PSM  E F+ +  +   AF +LG   E    +   H 
Sbjct: 305 VIKDILKAAYKEIGEEHVKMLESPSMGVESFAYFSMERPSAFYYLGCRNESKNIIYPAHG 364

Query: 367 AAFTIDESILEPGITMMAGIAAELLQ 392
           + F IDE  L  G+++    A + L+
Sbjct: 365 SLFDIDEDCLPIGVSIQCRAAYDFLK 390


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: 421
Number of extensions: 16
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: 390
Length adjustment: 31
Effective length of query: 363
Effective length of database: 359
Effective search space:   130317
Effective search space used:   130317
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