Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0019866 | organelle inner membrane | 4 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0031966 | mitochondrial membrane | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4IDV4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0016887 | ATP hydrolysis activity | 7 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.626 |
CLV_PCSK_FUR_1 | 311 | 315 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.628 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 71 | 77 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.351 |
DEG_MDM2_SWIB_1 | 231 | 238 | PF02201 | 0.420 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.547 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.490 |
DEG_SPOP_SBC_1 | 156 | 160 | PF00917 | 0.403 |
DEG_SPOP_SBC_1 | 425 | 429 | PF00917 | 0.667 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.474 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.593 |
DOC_CYCLIN_RxL_1 | 175 | 188 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 380 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 40 | 46 | PF00134 | 0.578 |
DOC_MAPK_DCC_7 | 180 | 189 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 311 | 321 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 402 | 408 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 500 | 510 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 257 | 266 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.330 |
DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.239 |
DOC_PP1_RVXF_1 | 504 | 511 | PF00149 | 0.433 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.424 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.351 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.626 |
DOC_PP2B_LxvP_1 | 540 | 543 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.664 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.468 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 459 | 465 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.392 |
LIG_Actin_WH2_2 | 214 | 232 | PF00022 | 0.414 |
LIG_BIR_III_2 | 66 | 70 | PF00653 | 0.526 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.403 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.352 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.323 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.330 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.411 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.405 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.351 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.540 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.696 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.474 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.514 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.377 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.390 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.420 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.432 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.467 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.402 |
LIG_GBD_Chelix_1 | 123 | 131 | PF00786 | 0.478 |
LIG_LIR_Gen_1 | 129 | 137 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 140 | 151 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 233 | 241 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 340 | 348 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.538 |
LIG_NRBOX | 45 | 51 | PF00104 | 0.479 |
LIG_NRBOX | 463 | 469 | PF00104 | 0.430 |
LIG_PCNA_yPIPBox_3 | 565 | 578 | PF02747 | 0.459 |
LIG_Pex14_1 | 349 | 353 | PF04695 | 0.369 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.370 |
LIG_REV1ctd_RIR_1 | 264 | 275 | PF16727 | 0.351 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.421 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.512 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 450 | 454 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.319 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.480 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 404 | 410 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 152 | 160 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 185 | 192 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 379 | 386 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 389 | 399 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 404 | 410 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 480 | 486 | PF11976 | 0.392 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.323 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.554 |
LIG_UBA3_1 | 334 | 339 | PF00899 | 0.496 |
LIG_UBA3_1 | 407 | 416 | PF00899 | 0.554 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.598 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.453 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.361 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.418 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.645 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.627 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.335 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.540 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.609 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.349 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.282 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.420 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.446 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.580 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.535 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.537 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.584 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.725 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.400 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.671 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.656 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.559 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.428 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.436 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.540 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.608 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.607 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.676 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.628 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.403 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.438 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.695 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.309 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.564 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.653 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.623 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.409 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.593 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.494 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.645 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.653 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.485 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.377 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.361 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.424 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.466 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.686 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.542 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.364 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.433 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.351 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.403 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.320 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.356 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.326 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.522 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.628 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.729 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.464 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.517 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.673 |
MOD_Plk_2-3 | 324 | 330 | PF00069 | 0.329 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.555 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.467 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.383 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.419 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.366 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.383 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.449 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.420 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.338 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.402 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.309 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.372 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.518 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.574 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.679 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.527 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 191 | 196 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 97 | 106 | PF00179 | 0.669 |
TRG_DiLeu_BaEn_1 | 478 | 483 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_3 | 330 | 336 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 477 | 482 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 563 | 568 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.585 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 578 | 581 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.617 |
TRG_ER_FFAT_2 | 129 | 140 | PF00635 | 0.278 |
TRG_NES_CRM1_1 | 310 | 324 | PF08389 | 0.420 |
TRG_NES_CRM1_1 | 373 | 386 | PF08389 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFP5 | Leptomonas seymouri | 70% | 100% |
A0A0S4IXD9 | Bodo saltans | 31% | 100% |
A0A1X0P1R2 | Trypanosomatidae | 41% | 100% |
A0A3Q8IUI9 | Leishmania donovani | 29% | 100% |
A0A3S7XBS4 | Leishmania donovani | 100% | 100% |
A4HAQ0 | Leishmania braziliensis | 27% | 100% |
A4HQ55 | Leishmania braziliensis | 85% | 100% |
C9ZVE3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A462 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ATX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
P32839 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
Q4Q0M1 | Leishmania major | 94% | 99% |
Q54DY9 | Dictyostelium discoideum | 30% | 100% |
Q54HY8 | Dictyostelium discoideum | 27% | 100% |
Q5E9H5 | Bos taurus | 28% | 100% |
Q7ZV60 | Danio rerio | 27% | 100% |
Q9CZP5 | Mus musculus | 27% | 100% |
Q9Y276 | Homo sapiens | 27% | 100% |
V5BUW7 | Trypanosoma cruzi | 41% | 100% |