GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Dyella japonica UNC79MFTsu3.2

Align ABC transporter for Lactose, ATPase component (characterized)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

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



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  333 bits (855), Expect = 3e-96
 Identities = 187/367 (50%), Positives = 245/367 (66%), Gaps = 15/367 (4%)

Query: 1   MSELQLSDVRKSYGGLEV-IKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSGD 59
           M++++L  +RK Y    V +     +I  GE +V VGPSGCGK+TLLRMIAGLE IS G 
Sbjct: 1   MAKVRLDKLRKVYPNGHVGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESISGGT 60

Query: 60  LTIDDVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAAH 119
           L+I +  +ND+ P  R IAMVFQ+YALYPHMTV EN+GF L+  G P+AEIE+RV EAA 
Sbjct: 61  LSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLRGQPKAEIERRVAEAAR 120

Query: 120 ILELGALLDRKPKQLSGGQRQRVAIGRAIVRHPKIFLFDEPLSNLDAELRVHMRIEIARL 179
           +LEL   LD +P  LSGGQRQRVA+GRA+VR PK+FL DEPLSNLDA+LR+ MR+EIAR+
Sbjct: 121 MLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRVEIARI 180

Query: 180 HKQLATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPKM 239
           H++L  T+VYVTHDQ+EAMTL  +IVV+  GV++Q+ +P++LYD PANLFVAGF+GSP M
Sbjct: 181 HQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFLGSPAM 240

Query: 240 NFLKGVIEIDEDQAYARLPD----YGDAKIPVTLQAAAGTAVTIGIRPEHF---DEAGPA 292
           N L+G++  D     A +P      G+      L+A     + +G+RPE      +A  A
Sbjct: 241 NLLRGILYRDGGWKLA-MPQGELVLGELPQGAALEAWRDRDIVVGLRPEDLLLCADAAGA 299

Query: 293 ALDLAIDMLEHLGGETFAYARHHGNGELIVVETKNGRGLKT-GDRLTARFDPVSVLVFD- 350
           AL   ++++E +G E F   RH   GEL +V     R L   G  L   F P  +  FD 
Sbjct: 300 ALAAQLEVVEPVGNEVFLNLRH---GELALVSRMPPRELPAPGSTLHFGFAPERLHFFDA 356

Query: 351 -GEGKRL 356
            GEG R+
Sbjct: 357 KGEGARI 363


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: 399
Number of extensions: 19
Number of successful extensions: 2
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: 364
Length adjustment: 29
Effective length of query: 329
Effective length of database: 335
Effective search space:   110215
Effective search space used:   110215
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 17 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