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 |
Related structures:
AlphaFold database: A4HD75
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0051301 | cell division | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
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_NRD_NRD_1 | 204 | 206 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.464 |
CLV_PCSK_PC7_1 | 368 | 374 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.609 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.404 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.606 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.531 |
DOC_CDC14_PxL_1 | 461 | 469 | PF14671 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 89 | 95 | PF00134 | 0.557 |
DOC_MAPK_DCC_7 | 18 | 28 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 289 | 298 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 454 | 464 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 490 | 497 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.271 |
DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.440 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.565 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.476 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 289 | 299 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 336 | 346 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 353 | 370 | PF00022 | 0.289 |
LIG_Actin_WH2_2 | 509 | 525 | PF00022 | 0.504 |
LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.365 |
LIG_EH1_1 | 289 | 297 | PF00400 | 0.420 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.493 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.685 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.372 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.363 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.384 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 460 | 466 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 105 | 112 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.408 |
LIG_MLH1_MIPbox_1 | 47 | 51 | PF16413 | 0.365 |
LIG_MYND_1 | 190 | 194 | PF01753 | 0.443 |
LIG_NRBOX | 140 | 146 | PF00104 | 0.412 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.386 |
LIG_NRBOX | 311 | 317 | PF00104 | 0.397 |
LIG_NRBOX | 419 | 425 | PF00104 | 0.271 |
LIG_NRBOX | 48 | 54 | PF00104 | 0.250 |
LIG_PCNA_yPIPBox_3 | 454 | 462 | PF02747 | 0.335 |
LIG_PCNA_yPIPBox_3 | 510 | 523 | PF02747 | 0.417 |
LIG_Pex14_1 | 104 | 108 | PF04695 | 0.437 |
LIG_Pex14_2 | 479 | 483 | PF04695 | 0.378 |
LIG_REV1ctd_RIR_1 | 477 | 486 | PF16727 | 0.412 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.436 |
LIG_SH2_PTP2 | 463 | 466 | PF00017 | 0.289 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.405 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.541 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.281 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.404 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 132 | 138 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.314 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.459 |
LIG_UBA3_1 | 49 | 57 | PF00899 | 0.416 |
LIG_WRC_WIRS_1 | 65 | 70 | PF05994 | 0.452 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.562 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.487 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.495 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.589 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.503 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.605 |
MOD_DYRK1A_RPxSP_1 | 375 | 379 | PF00069 | 0.284 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.383 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.658 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.288 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.408 |
MOD_GlcNHglycan | 518 | 522 | PF01048 | 0.427 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.540 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.495 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.504 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.489 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.564 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.541 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.497 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.292 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.302 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.289 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.465 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.517 |
MOD_N-GLC_2 | 238 | 240 | PF02516 | 0.494 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.427 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.407 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.563 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.660 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.617 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.526 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.330 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.428 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.484 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.437 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.436 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.350 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.448 |
MOD_OFUCOSY | 3 | 10 | PF10250 | 0.429 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.428 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.572 |
MOD_PK_1 | 129 | 135 | PF00069 | 0.518 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.521 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.350 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.435 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.420 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.335 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.416 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.477 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.437 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.389 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.621 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.513 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.346 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.430 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.331 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.560 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.627 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.303 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.469 |
TRG_DiLeu_BaEn_2 | 260 | 266 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 202 | 207 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 233 | 244 | PF08389 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.193 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NKH8 | Trypanosomatidae | 35% | 100% |
A0A1X0NXH5 | Trypanosomatidae | 26% | 79% |
A0A3Q8IG04 | Leishmania donovani | 84% | 100% |
A0A3R7MBQ6 | Trypanosoma rangeli | 38% | 100% |
D0A6Y7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AH29 | Leishmania infantum | 84% | 100% |
E9AWK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAW3 | Leishmania major | 83% | 100% |
V5BRB9 | Trypanosoma cruzi | 40% | 100% |