GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Pseudomonas stutzeri RCH2

Align ABC transporter for Lactose, ATPase component (characterized)
to candidate GFF1860 Psest_1899 ABC-type sugar transport systems, ATPase components

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



>FitnessBrowser__psRCH2:GFF1860
          Length = 390

 Score =  310 bits (795), Expect = 3e-89
 Identities = 173/367 (47%), Positives = 241/367 (65%), Gaps = 13/367 (3%)

Query: 1   MSELQLSDVRKSYGGLEV--IKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSG 58
           M+ L+L +V+KSYG  ++  +K + L I +GEF++ VGPSGCGKSTL+  IAGLE I+ G
Sbjct: 1   MASLELRNVQKSYGNSQIATLKDIALKIDAGEFLILVGPSGCGKSTLMNCIAGLENITGG 60

Query: 59  DLTIDDVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAA 118
           ++ +D   ++   P  R IAMVFQSYALYP M+VR+N+ F L+   VP A+IE+ V   A
Sbjct: 61  EILVDGEDISQASPKDRDIAMVFQSYALYPTMSVRDNIAFGLKMRKVPAAKIEEEVARVA 120

Query: 119 HILELGALLDRKPKQLSGGQRQRVAIGRAIVRHPKIFLFDEPLSNLDAELRVHMRIEIAR 178
            +L++  LL+RKP QLSGGQ+QRVA+GRA+ R PKI+LFDEPLSNLDA+LRV MR EI  
Sbjct: 121 KLLQIEPLLERKPSQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEIKL 180

Query: 179 LHKQLATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPK 238
           +H++L TT VYVTHDQ+EAMTL DK+ VM+ GV++Q G+P ++Y++PANLFVA FIGSP 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGVIQQFGTPHEIYNNPANLFVASFIGSPP 240

Query: 239 MNFLKGVIEIDEDQAYARL-PDYGDAKIPVTLQAAAG---TAVTIGIRPEHFD--EAGPA 292
           MNF+   I   + +    L  + G  ++P+ + +  G     + +GIRPE      AG A
Sbjct: 241 MNFVPLRIRQRDGRWVGVLNSEQGSCELPLPITSDDGLRDRELILGIRPEQIGLAPAGSA 300

Query: 293 ALDLAID--MLEHLGGETFAYARHHGNGELIVVETKNGRGLKTGDRLTARFDPVSVLVFD 350
              LA+D  ++E  G +T        N           +  + G+ L  +FDP   L+FD
Sbjct: 301 DFSLAVDIEVVEPTGPDTLVVFTL--NQVKACCRLAPDQAPRVGETLNLQFDPRRALLFD 358

Query: 351 GE-GKRL 356
            + G+RL
Sbjct: 359 AQTGERL 365


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: 386
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: 390
Length adjustment: 30
Effective length of query: 328
Effective length of database: 360
Effective search space:   118080
Effective search space used:   118080
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: 50 (23.9 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