GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Jannaschia aquimarina GSW-M26

Align ABC transporter for Lactose, ATPase component (characterized)
to candidate WP_043917711.1 jaqu_RS04170 ABC transporter ATP-binding protein

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



>NCBI__GCF_000877395.1:WP_043917711.1
          Length = 344

 Score =  335 bits (859), Expect = 1e-96
 Identities = 191/354 (53%), Positives = 236/354 (66%), Gaps = 23/354 (6%)

Query: 2   SELQLSDVRKSYGGLEVIKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSGDLT 61
           ++++L  V K +G  +VIKGVDL + +GEFVVFVGPSGCGKSTLLRMIAGLEE S G + 
Sbjct: 3   AQVELVGVEKWFGDAQVIKGVDLAVAAGEFVVFVGPSGCGKSTLLRMIAGLEETSRGQIL 62

Query: 62  IDDVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAAHIL 121
           ++        PSKRG+AMVFQSYALYPH++VREN+GF L+ AG+ + EI  RV+EAA  L
Sbjct: 63  VEGRDATAEPPSKRGLAMVFQSYALYPHLSVRENVGFPLKAAGMSKDEISARVDEAARAL 122

Query: 122 ELGALLDRKPKQLSGGQRQRVAIGRAIVRHPKIFLFDEPLSNLDAELRVHMRIEIARLHK 181
            L   LDR+PK LSGGQRQRVAIGR+IVR P  FLFDEPLSNLDA LRV MR EIA+LH+
Sbjct: 123 RLTDYLDRRPKDLSGGQRQRVAIGRSIVREPVAFLFDEPLSNLDAALRVEMRYEIAKLHQ 182

Query: 182 QLATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPKMNF 241
           QL T ++YVTHDQ+EAMTLAD+IVV+ AG + QVG+P +LY  P +LFVA FIGSPKMN 
Sbjct: 183 QLGTAMIYVTHDQIEAMTLADRIVVLEAGRIAQVGTPRELYLRPRSLFVAQFIGSPKMN- 241

Query: 242 LKGVIEIDEDQAYARLPDYGDAKIPVTLQAAAGTAVTIGIRPEHFDEA--GPAALDLAID 299
              V   D       +PD         L A  G A T+G+RPE    A  G   L  ++D
Sbjct: 242 ---VFTAD------AVPD---------LDAPPG-AATLGVRPEDLRIAPQGDGGLSGSVD 282

Query: 300 MLEHLGGETFAYARHHGNGELIVVETKNGRGLKTGDRLTARFDPVSVLVFDGEG 353
           +LE+LG +TF      G    I        GL  G+ +   FD  ++  FD +G
Sbjct: 283 VLEYLGADTFVIV-DCGPAGRITARVPGEAGLAPGEAVALEFDRSALHAFDEKG 335


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: 384
Number of extensions: 18
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: 344
Length adjustment: 29
Effective length of query: 329
Effective length of database: 315
Effective search space:   103635
Effective search space used:   103635
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.

Links

Downloads

Related tools

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