GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Clostridium kluyveri DSM 555

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

Query= predicted:L0FXC2
         (397 letters)



>NCBI__GCF_000016505.1:WP_012101872.1
          Length = 390

 Score =  294 bits (752), Expect = 3e-84
 Identities = 156/379 (41%), Positives = 228/379 (60%), Gaps = 5/379 (1%)

Query: 16  QTIAIRRHIHAHPELSFEEHQTCAFVEKHLQEIGITNIQRKANTGLVALIEGKNPSKKVI 75
           + I IRR +H HPEL +EE +T   +++ L++IGI  ++  A TG+  +I GK    K I
Sbjct: 15  ELIDIRRDLHRHPELGYEEERTSFKIKEFLKKIGIEYMET-AGTGVCGIIRGKG--NKTI 71

Query: 76  ALRADMDALPIVEQNDVPYKSNKEGVMHACGHDVHTSSLLGAASILHAVKDQFEGTVKLI 135
            +RAD+DALP+ +  +  Y S  +G MHACGHD HT+ LLG A +L++VKD+ +GTVKL 
Sbjct: 72  GIRADIDALPLEDHKNCSYSSKVKGKMHACGHDAHTTILLGTAKVLNSVKDELKGTVKLF 131

Query: 136 FQPGEEKIPGGASLMIKDKALENPRPSGIVGQHVMPLIDAGKVGFRKGMYMASADELYLK 195
           F+P EE   GGA LM+K+ ALENPR   ++G HV   I+ G +G + G+  A+++   +K
Sbjct: 132 FEPAEETT-GGAKLMVKEGALENPRVDRVIGLHVDENIEVGNIGVKLGVVNAASNPFTIK 190

Query: 196 VIGKGGHGAMPETLVDPVLIASHIIVALQQVISRNASPKVPSVLSFGRIEALGATNVIPN 255
           + G G HGA P   VDP++I+SH+I+ALQQ++SR   P   +V++ G I    A N+IP 
Sbjct: 191 IKGVGAHGARPHMGVDPIVISSHVILALQQIVSRELPPTDAAVITVGSIHGGTAQNIIPE 250

Query: 256 EVNIQGTFRTLDETWRAEAHQKMVKIAEGIAEGMGGSVDFEVRKGYPFLQNAPELTDRAY 315
           EV I GT RT+    R    +++ +I  G+   M G  + ++ + YP L N  ++     
Sbjct: 251 EVVIAGTMRTMRTEHREYVKERLREITFGVVNSMRGKYEIDIEESYPCLYNDDDVIKDIL 310

Query: 316 KAAQAYLGEENVEDLDI-WMAAEDFSYYTQEMDGCFYRLGIRNEEKGITSGVHTPTFDID 374
           KAA   +GEE+V+ L+   M  E F+Y++ E    FY LG RNE K I    H   FDID
Sbjct: 311 KAAYKEIGEEHVKMLESPSMGVESFAYFSMERPSAFYYLGCRNESKNIIYPAHGSLFDID 370

Query: 375 ESALEVGAGLMAWIAINEL 393
           E  L +G  +    A + L
Sbjct: 371 EDCLPIGVSIQCRAAYDFL 389


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: 389
Number of extensions: 22
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