Align Inositol transport system ATP-binding protein (characterized)
to candidate H281DRAFT_00426 H281DRAFT_00426 monosaccharide ABC transporter ATP-binding protein, CUT2 family
Query= reanno::WCS417:GFF2332 (517 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_00426 H281DRAFT_00426 monosaccharide ABC transporter ATP-binding protein, CUT2 family Length = 503 Score = 458 bits (1178), Expect = e-133 Identities = 245/492 (49%), Positives = 334/492 (67%), Gaps = 3/492 (0%) Query: 23 LLEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDAGEIRL 82 L+ + +SK FPGV AL DVQ + G V ALMGENGAGKSTLMKI+AG+Y D+GEI L Sbjct: 4 LISVKKLSKSFPGVRALHDVQFDLVEGEVHALMGENGAGKSTLMKILAGVYTRDSGEILL 63 Query: 83 RGKPIVFETPLAAQKAGIAMIHQELNLMPHMSIAENIWIGREQLNSLHM-VNHREMHRCT 141 G+P+ ++P AQ AGI +IHQEL LM H+++A+NI+IGRE L + ++ +++ Sbjct: 64 GGQPVELQSPRDAQAAGIGIIHQELQLMNHLTVAQNIFIGREPRGRLGLFLDEDKLNAKA 123 Query: 142 AELLARLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVAHLFS 201 E+L+R+ +N+DP VGNL++A +QMVEIAKA+S+DS +LIMDEPTSA+ + E+A LF Sbjct: 124 REILSRMHVNIDPRAMVGNLTVASQQMVEIAKALSFDSRVLIMDEPTSALNDAEIAELFR 183 Query: 202 IIADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMVGREL 261 II +LK +G G+VYI+HKM+E+ IAD V V RDG Y+ A + +++I MMVGR L Sbjct: 184 IIRELKQRGVGVVYISHKMDELKQIADRVTVLRDGEYVATVAAADTSVEAIIGMMVGRTL 243 Query: 262 SQLFPL-RETPIGDLLLTVRDLTLDGVFKDVSFDLHAGEILGIAGLMGSGRTNVAETIFG 320 S + P R G++ L VR+L + +DVSF L GEILG AGLMG+GRT VA +FG Sbjct: 244 SDVAPAGRAASQGEIALEVRNLHAGPLVRDVSFTLRKGEILGFAGLMGAGRTEVARAVFG 303 Query: 321 ITPSSSGQITLDGKAVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVLPHYT 380 P SG+I + G I P A+ G L+EDRK GL + V N+ M+ L ++ Sbjct: 304 ADPVESGEIFVKGAKASIRTPSDAVAHGIGYLSEDRKRFGLATGMDVESNIVMSNLRNFL 363 Query: 381 G-NGFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTNPRLLILD 439 N F+++ +R L ++TPS Q + LSGGNQQK ++A+WL + +L D Sbjct: 364 SLNFFLRRARMRRRASHFINLLAIRTPSAAQQVRLLSGGNQQKIVIAKWLERDCDVLFFD 423 Query: 440 EPTRGIDVGAKAEIYRLIAFLASEGMAVIMISSELPEVLGMSDRVMVMHEGELMGTLDRS 499 EPTRGIDVGAK+EIY+L+ LA EG A++MISSELPE+L MSDRV+VM EG + G L Sbjct: 424 EPTRGIDVGAKSEIYKLLRSLADEGKAIVMISSELPEILRMSDRVVVMCEGRITGELPAE 483 Query: 500 EATQEKVMQLAS 511 +ATQE++M LA+ Sbjct: 484 QATQERIMHLAT 495 Score = 101 bits (251), Expect = 7e-26 Identities = 61/225 (27%), Positives = 118/225 (52%), Gaps = 4/225 (1%) Query: 290 DVSFDLHAGEILGIAGLMGSGRTNVAETIFGITPSSSGQITLDGKAVRISDPHMAIEKGF 349 DV FDL GE+ + G G+G++ + + + G+ SG+I L G+ V + P A G Sbjct: 22 DVQFDLVEGEVHALMGENGAGKSTLMKILAGVYTRDSGEILLGGQPVELQSPRDAQAAGI 81 Query: 350 ALLTEDRKLSGLFPCLSVLENMEMAVLPHYTGNGFIQQKALRALCEDMCKKLRVKTPSLE 409 ++ ++ +L L+V +N+ + P F+ + L A ++ ++ V Sbjct: 82 GIIHQELQLMNH---LTVAQNIFIGREPRGRLGLFLDEDKLNAKAREILSRMHVNIDP-R 137 Query: 410 QCIDTLSGGNQQKALLARWLMTNPRLLILDEPTRGIDVGAKAEIYRLIAFLASEGMAVIM 469 + L+ +QQ +A+ L + R+LI+DEPT ++ AE++R+I L G+ V+ Sbjct: 138 AMVGNLTVASQQMVEIAKALSFDSRVLIMDEPTSALNDAEIAELFRIIRELKQRGVGVVY 197 Query: 470 ISSELPEVLGMSDRVMVMHEGELMGTLDRSEATQEKVMQLASGMT 514 IS ++ E+ ++DRV V+ +GE + T+ ++ + E ++ + G T Sbjct: 198 ISHKMDELKQIADRVTVLRDGEYVATVAAADTSVEAIIGMMVGRT 242 Score = 86.3 bits (212), Expect = 2e-21 Identities = 63/243 (25%), Positives = 110/243 (45%), Gaps = 10/243 (4%) Query: 24 LEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDAGEIRLR 83 LE+ N+ G + DV +R G +L G GAG++ + + + G ++GEI ++ Sbjct: 260 LEVRNLHAG----PLVRDVSFTLRKGEILGFAGLMGAGRTEVARAVFGADPVESGEIFVK 315 Query: 84 GKPIVFETPLAAQKAGIAMIHQE---LNLMPHMSIAENIWIG--REQLNSLHMVNHREMH 138 G TP A GI + ++ L M + NI + R L+ + M Sbjct: 316 GAKASIRTPSDAVAHGIGYLSEDRKRFGLATGMDVESNIVMSNLRNFLSLNFFLRRARMR 375 Query: 139 RCTAELLARLRINL-DPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVA 197 R + + L I +QV LS +Q + IAK + D D+L DEPT I + Sbjct: 376 RRASHFINLLAIRTPSAAQQVRLLSGGNQQKIVIAKWLERDCDVLFFDEPTRGIDVGAKS 435 Query: 198 HLFSIIADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMV 257 ++ ++ L +GK IV I+ ++ E+ ++D V V +G G A+ + ++ + Sbjct: 436 EIYKLLRSLADEGKAIVMISSELPEILRMSDRVVVMCEGRITGELPAEQATQERIMHLAT 495 Query: 258 GRE 260 R+ Sbjct: 496 QRQ 498 Lambda K H 0.320 0.136 0.381 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: 569 Number of extensions: 23 Number of successful extensions: 8 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 3 Length of query: 517 Length of database: 503 Length adjustment: 34 Effective length of query: 483 Effective length of database: 469 Effective search space: 226527 Effective search space used: 226527 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: 52 (24.6 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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:
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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