GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Nocardioides daejeonensis MJ31

Align ABC transporter for Lactose, ATPase component (characterized)
to candidate WP_110206994.1 DNK54_RS11055 ABC transporter ATP-binding protein

Query= reanno::Smeli:SM_b20002
         (358 letters)



>NCBI__GCF_003194585.1:WP_110206994.1
          Length = 368

 Score =  233 bits (593), Expect = 8e-66
 Identities = 138/368 (37%), Positives = 212/368 (57%), Gaps = 27/368 (7%)

Query: 2   SELQLSDVRKSYGGLEVIKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSGDLT 61
           + +++  +RK YG   ++  +DLDI++GEF+  +G SG GKSTLL +IAG  +   GD+ 
Sbjct: 14  ASIEVDRIRKVYGSTTILNDIDLDIRAGEFLTLLGASGSGKSTLLNIIAGFIKADGGDVR 73

Query: 62  IDDVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAAHIL 121
           +D   +  V   KRG+ MVFQ YAL+PHM+V +N+ + LR  G P+AEI   V +A  ++
Sbjct: 74  VDGKSITSVPAHKRGLGMVFQHYALFPHMSVYDNVAYGLRRHGFPKAEIPGLVADALEMV 133

Query: 122 ELGALLDRKPKQLSGGQRQRVAIGRAIVRHPKIFLFDEPLSNLDAELRVHMRIEIARLHK 181
           E+G L  R+P +LSGGQ+QRVA+ RA+V  P++ L DEPL  LD  LR  +++EI RLHK
Sbjct: 134 EMGHLGKRRPAELSGGQQQRVALARAVVFRPRVLLMDEPLGALDKMLREQLQLEIRRLHK 193

Query: 182 QLATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPKMNF 241
           ++  T V+VTHDQ EA+T++D+I ++  G + Q+G+P +LYD P+  + A FIG    N 
Sbjct: 194 EMGITFVFVTHDQEEALTMSDRIALLEKGDIVQLGTPEELYDAPSCRYAAEFIG--VSNI 251

Query: 242 LKGVIEIDEDQAYARLPD-YGDAKIPVTLQAAAGTA--VTIGIRPEHF----DEAGPA-- 292
           + G          +R  D + D +   T + + G A    + +RPE       + GPA  
Sbjct: 252 MTG----------SRAGDVFTDTRNQTTHKVSGGAADGTVLMVRPERLRVSAGQVGPAGH 301

Query: 293 --ALDLAIDMLEHLGGETFAYARHHGNGELIVVETKNGR---GLKTGDRLTARFDPVSVL 347
             AL   +    +LG +   + R   +GE +V  T+  R   G++ G  +T  ++     
Sbjct: 302 ENALPAIVSDCVYLGSDRTVHVR-TASGEEMVARTEVPRTDDGIQPGVPVTLTWNIEDAR 360

Query: 348 VFDGEGKR 355
           V   E  R
Sbjct: 361 VLAEEAAR 368


Lambda     K      H
   0.321    0.139    0.396 

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: 369
Number of extensions: 15
Number of successful extensions: 1
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: 358
Length of database: 368
Length adjustment: 29
Effective length of query: 329
Effective length of database: 339
Effective search space:   111531
Effective search space used:   111531
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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