GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Acidovorax sp. GW101-3H11

Align LacK, component of Lactose porter (characterized)
to candidate Ac3H11_4785 Glycerol-3-phosphate ABC transporter, ATP-binding protein UgpC (TC 3.A.1.1.3)

Query= TCDB::Q01937
         (363 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4785
          Length = 334

 Score =  321 bits (823), Expect = 2e-92
 Identities = 191/366 (52%), Positives = 231/366 (63%), Gaps = 38/366 (10%)

Query: 1   MAEVRLTDIRKSYG----SLEVIKGVNLEVSSGEFVVFVGPSGCGKSTLLRMIAGLEDIS 56
           MA + L +I K YG    + +VI GVN EV  GEFVV VGPSGCGKSTLLRM+AGLE+IS
Sbjct: 1   MASLSLRNITKRYGHGPKANQVIHGVNAEVKDGEFVVIVGPSGCGKSTLLRMVAGLEEIS 60

Query: 57  SGELTIGGTVMNDVDPSKRGIAMVFQTYALYPHMTVRENMGFALRFAGMAKDEIERRVNA 116
            GEL IG  V+ND++P++R IAMVFQ YALYPHMT  ENM + L+ A + KDEI+ RV+ 
Sbjct: 61  GGELRIGDRVVNDLEPAQRDIAMVFQNYALYPHMTNFENMAYGLKIAKVPKDEIKARVDK 120

Query: 117 AAKILELDALMDRKPKALSGGQRQRVAIGRAIVRQPDVFLFDEPLSNLDAELRVHMRVEI 176
           AAKILEL  L++RKP+ LSGGQRQRVA+GRAIVRQP VFLFDEPLSNLDA+LR   R+EI
Sbjct: 121 AAKILELGHLLERKPRELSGGQRQRVAMGRAIVRQPQVFLFDEPLSNLDAKLRAQTRLEI 180

Query: 177 ARLHKELNATIVYVTHDQVEAMTLADKIVVMRGGIVEQVGAPLALYDDPDNMFVAGFIGS 236
            +LH+EL  T ++VTHDQVEAMTLA +++VM  G +EQ G P  +Y  P   FVA FIGS
Sbjct: 181 QKLHRELGITSLFVTHDQVEAMTLAQRMIVMNAGNMEQFGTPEEVYHTPATTFVASFIGS 240

Query: 237 PRMNFLPAVVIGQAEGGQVTVALKARPDTQLTVACATPPQGGDAVTVGVRPEHFLPAGSG 296
           P MN L       A G        A+P T L                G+RPEH      G
Sbjct: 241 PPMNLLK-----NAPG--------AQPGTIL----------------GIRPEHLDVRSEG 271

Query: 297 DTQLTAHVDVVEHLGNTSYVYAHTVPGEQIIIEQEERRHGGRYGDEIAVGISAKTSFLFD 356
                  V+ VE LG    +Y   + GEQ+I+  EE  H       I V   A     FD
Sbjct: 272 ---WAVTVETVELLGAERLIYGR-INGEQVIVRVEEGTHSPEPDSVIHVQPRADRLHAFD 327

Query: 357 -ASGRR 361
            A+G+R
Sbjct: 328 AATGKR 333


Lambda     K      H
   0.320    0.137    0.390 

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: 340
Number of extensions: 9
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: 363
Length of database: 334
Length adjustment: 29
Effective length of query: 334
Effective length of database: 305
Effective search space:   101870
Effective search space used:   101870
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