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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H5L4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.323 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.509 |
DOC_ANK_TNKS_1 | 14 | 21 | PF00023 | 0.364 |
DOC_ANK_TNKS_1 | 437 | 444 | PF00023 | 0.440 |
DOC_CKS1_1 | 448 | 453 | PF01111 | 0.554 |
DOC_CYCLIN_RxL_1 | 345 | 355 | PF00134 | 0.511 |
DOC_CYCLIN_RxL_1 | 68 | 77 | PF00134 | 0.531 |
DOC_CYCLIN_RxL_1 | 86 | 94 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 133 | 142 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 248 | 256 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.478 |
DOC_MAPK_RevD_3 | 73 | 87 | PF00069 | 0.402 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.484 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.646 |
LIG_14-3-3_CterR_2 | 461 | 464 | PF00244 | 0.436 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.531 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.312 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.481 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.534 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.502 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.395 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.466 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.545 |
LIG_Integrin_RGD_1 | 15 | 17 | PF01839 | 0.407 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.500 |
LIG_MAD2 | 138 | 146 | PF02301 | 0.446 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.450 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.553 |
LIG_SH2_SRC | 97 | 100 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.438 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.461 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.657 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.331 |
LIG_SH3_4 | 145 | 152 | PF00018 | 0.616 |
LIG_SUMO_SIM_par_1 | 452 | 460 | PF11976 | 0.373 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.374 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.346 |
LIG_TYR_ITSM | 421 | 428 | PF00017 | 0.552 |
LIG_UBA3_1 | 454 | 462 | PF00899 | 0.575 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.510 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.652 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.582 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.387 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.477 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.453 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.688 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.447 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.329 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.556 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.557 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.653 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.576 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.667 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.445 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.554 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.560 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.474 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.612 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.542 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.693 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.635 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.543 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.300 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.511 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.554 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.358 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.621 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.614 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.608 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.410 |
MOD_PK_1 | 222 | 228 | PF00069 | 0.614 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.649 |
MOD_PKA_1 | 300 | 306 | PF00069 | 0.703 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.531 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.531 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.649 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.627 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.771 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.570 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.538 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.513 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.531 |
MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.503 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.642 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.583 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.625 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.300 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.723 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.604 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.504 |
MOD_SUMO_for_1 | 381 | 384 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 355 | 361 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 93 | 98 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_2 | 203 | 209 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.563 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 89 | 93 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2N2 | Leptomonas seymouri | 55% | 99% |
A0A1X0NPB5 | Trypanosomatidae | 24% | 100% |
A0A3R7K7T1 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WQL0 | Leishmania donovani | 77% | 100% |
A4HTV2 | Leishmania infantum | 76% | 78% |
D0A9B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AMP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QHY6 | Leishmania major | 79% | 100% |