GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Clostridium tyrobutyricum FAM22553

Align Predicted dapE by GapMind curators (no experimental data)
to candidate WP_017750568.1 PN53_RS01465 M20 family metallopeptidase

Query= predicted:L0FXC2
         (397 letters)



>NCBI__GCF_000816635.1:WP_017750568.1
          Length = 390

 Score =  288 bits (738), Expect = 1e-82
 Identities = 149/378 (39%), Positives = 224/378 (59%), Gaps = 5/378 (1%)

Query: 8   KLAADQLNQTIAIRRHIHAHPELSFEEHQTCAFVEKHLQEIGITNIQRKANTGLVALIEG 67
           K+A +  ++ + +RR IH HPEL +E ++T   ++  L +  I  ++  A +G+ A+I G
Sbjct: 7   KMARNMQDELVKVRRDIHMHPELDYELYRTQGKIKDVLDKENIEYVE-SAGSGICAIIRG 65

Query: 68  KNPSKKVIALRADMDALPIVEQNDVPYKSNKEGVMHACGHDVHTSSLLGAASILHAVKDQ 127
                K I LRADMDALP+ +     Y S ++G MHACGHD HT+ LLG A IL+ +KDQ
Sbjct: 66  NG--SKTIGLRADMDALPLQDMKKCDYASKEKGKMHACGHDAHTTILLGVAKILNRIKDQ 123

Query: 128 FEGTVKLIFQPGEEKIPGGASLMIKDKALENPRPSGIVGQHVMPLIDAGKVGFRKGMYMA 187
             G VKL F+P EE   GGA +MIK+  LE+P    ++G HV   ID GK+G R G+  A
Sbjct: 124 LNGNVKLFFEPAEET-SGGAKVMIKEGVLESPHVDRVIGLHVEEGIDVGKIGVRYGVVNA 182

Query: 188 SADELYLKVIGKGGHGAMPETLVDPVLIASHIIVALQQVISRNASPKVPSVLSFGRIEAL 247
           +++   +K+ G G HGA P T +DP+++ S+++VALQ++ISR   P   ++++ G I   
Sbjct: 183 ASNPFNIKIKGIGAHGARPHTGIDPIVMGSYVVVALQEIISREIPPTDGALITVGSIHGG 242

Query: 248 GATNVIPNEVNIQGTFRTLDETWRAEAHQKMVKIAEGIAEGMGGSVDFEVRKGYPFLQNA 307
            A N+IP E+ I G  RT+    R    +++ ++ EGI + M GS + E+ + YP L N 
Sbjct: 243 TAQNIIPTELTIAGIIRTMKTEHREYVKKRLREVTEGIVKSMRGSCEIEIEESYPCLYND 302

Query: 308 PELTDRAYKAAQAYLGEENVEDL-DIWMAAEDFSYYTQEMDGCFYRLGIRNEEKGITSGV 366
             +      +A   +G+EN+ DL +  M  E F+Y++      FY LG RNE +GIT+  
Sbjct: 303 DTVIKNVVSSASKIIGDENIVDLKNPSMGVESFAYFSMNRPSAFYYLGSRNESRGITNPA 362

Query: 367 HTPTFDIDESALEVGAGL 384
           H   FDIDE  L +G  +
Sbjct: 363 HGNLFDIDEECLPIGVAI 380


Lambda     K      H
   0.317    0.134    0.387 

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: 406
Number of extensions: 20
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: 397
Length of database: 390
Length adjustment: 31
Effective length of query: 366
Effective length of database: 359
Effective search space:   131394
Effective search space used:   131394
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 (21.6 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