GapMind for catabolism of small carbon sources

 

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

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate WP_043916916.1 jaqu_RS00215 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::psRCH2:GFF857
         (371 letters)



>NCBI__GCF_000877395.1:WP_043916916.1
          Length = 372

 Score =  336 bits (861), Expect = 7e-97
 Identities = 196/366 (53%), Positives = 240/366 (65%), Gaps = 12/366 (3%)

Query: 1   MASVTLRDICKSYDG-TPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGD 59
           MA++ L+D+ K Y G   + + IDLDIE GE +VFVGPSGCGKSTLLR+IAGLE I+ G 
Sbjct: 1   MANLKLKDVAKVYGGQVEVLKDIDLDIETGELIVFVGPSGCGKSTLLRMIAGLEQISGGT 60

Query: 60  LLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAE 119
           L ID   VND+PP +R + MVFQSYALYPHMTV +NMAF L++A   K EI R V A A+
Sbjct: 61  LEIDGMVVNDVPPSERGIAMVFQSYALYPHMTVYDNMAFALQIAKKSKEEIDRAVRAAAD 120

Query: 120 ILQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARL 179
            LQL + L+R PK LSGGQRQRVAIGR++VR+PKV+LFDEPLSNLDA LRV  RIEIA+L
Sbjct: 121 KLQLTEYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRIEIAQL 180

Query: 180 HQRI-RSTMIYVTHDQVEAMTLADKIVVLNA-------GEIAQVGQPLHLYHYPKNRFVA 231
            +++  STMIYVTHDQVEAMTLA +IVVL+A         IAQVG PL LY  P + FVA
Sbjct: 181 KEQMPDSTMIYVTHDQVEAMTLASRIVVLDALKDNGYKYSIAQVGTPLELYETPNSEFVA 240

Query: 232 GFLGSPQMNFVEVRAISASPETVTIELPSGY-PLTLPVDGSAVSPGDPLTLGIRPEHFVM 290
            F+GSP MN +E   I A+ ET T+    G   +T  V       G  + +GIRPE  V 
Sbjct: 241 RFIGSPAMNLLE-GEIVATGETTTLRTRLGAGTITSNVPSRPEDQGAQVKVGIRPEDAVA 299

Query: 291 PDEADFTFHGQITVAERLGQYNLLYLTLERLQ-DVITLCVDGNLRVTEGETFAAGLKADK 349
            D  DF F G++ V ERLG+  LLY      Q D +   + G      G T        K
Sbjct: 300 TDSEDFAFSGKVEVEERLGEVTLLYFERGAGQNDPVIAKLPGIHPGMRGNTVKLTADPAK 359

Query: 350 CHLFRE 355
            H+F++
Sbjct: 360 VHIFQD 365


Lambda     K      H
   0.322    0.139    0.405 

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: 402
Number of extensions: 18
Number of successful extensions: 3
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: 371
Length of database: 372
Length adjustment: 30
Effective length of query: 341
Effective length of database: 342
Effective search space:   116622
Effective search space used:   116622
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 (21.9 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