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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QHV4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 214 | 218 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.688 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.652 |
CLV_PCSK_PC7_1 | 351 | 357 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.548 |
CLV_Separin_Fungi | 346 | 352 | PF03568 | 0.590 |
DEG_Kelch_Keap1_1 | 25 | 30 | PF01344 | 0.504 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.631 |
DEG_SCF_FBW7_1 | 6 | 12 | PF00400 | 0.540 |
DEG_SCF_FBW7_2 | 71 | 76 | PF00400 | 0.569 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.755 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.537 |
DOC_MAPK_gen_1 | 187 | 194 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 195 | 202 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 252 | 262 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 187 | 194 | PF00069 | 0.576 |
DOC_PP4_MxPP_1 | 366 | 369 | PF00568 | 0.644 |
DOC_SPAK_OSR1_1 | 307 | 311 | PF12202 | 0.651 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.655 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.688 |
LIG_APCC_ABBAyCdc20_2 | 231 | 237 | PF00400 | 0.406 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.628 |
LIG_CtBP_PxDLS_1 | 448 | 452 | PF00389 | 0.596 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.634 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.601 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.545 |
LIG_GBD_Chelix_1 | 31 | 39 | PF00786 | 0.545 |
LIG_LIR_Apic_2 | 375 | 380 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 442 | 448 | PF02991 | 0.611 |
LIG_LIR_Apic_2 | 97 | 101 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.682 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.562 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.503 |
LIG_SH2_CRK | 378 | 382 | PF00017 | 0.686 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.647 |
LIG_SH2_GRB2like | 377 | 380 | PF00017 | 0.616 |
LIG_SH2_PTP2 | 445 | 448 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.649 |
LIG_SH2_STAT3 | 155 | 158 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.606 |
LIG_SH3_2 | 6 | 11 | PF14604 | 0.609 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.744 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.599 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.659 |
LIG_SUMO_SIM_anti_2 | 450 | 455 | PF11976 | 0.594 |
LIG_SUMO_SIM_par_1 | 447 | 452 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.608 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.536 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.604 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.548 |
MOD_CDK_SPxK_1 | 334 | 340 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 5 | 11 | PF00069 | 0.534 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.561 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.599 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.571 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.514 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.730 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.726 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.596 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.634 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.576 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.785 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.559 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.676 |
MOD_Cter_Amidation | 195 | 198 | PF01082 | 0.640 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.520 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.628 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.535 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.643 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.688 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.619 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.594 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.582 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.655 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.647 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.685 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.734 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.589 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.629 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.639 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.700 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.754 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.634 |
MOD_LATS_1 | 409 | 415 | PF00433 | 0.614 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.644 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.686 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.629 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.726 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.644 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.573 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.674 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.636 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.638 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.665 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.537 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.598 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.644 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.617 |
MOD_NEK2_2 | 392 | 397 | PF00069 | 0.552 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.597 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.579 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.627 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.671 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.654 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.626 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.546 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.563 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.739 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.710 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.591 |
MOD_PKB_1 | 349 | 357 | PF00069 | 0.589 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.642 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.719 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.607 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.576 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.551 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.714 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.599 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.643 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.642 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.599 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.632 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.666 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.635 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.729 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.683 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 228 | 232 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 30 | 38 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 56 | 64 | PF00179 | 0.582 |
TRG_DiLeu_BaEn_4 | 239 | 245 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.686 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQN7 | Leishmania donovani | 76% | 89% |
A4H5Q1 | Leishmania braziliensis | 42% | 100% |
A4HTZ1 | Leishmania infantum | 76% | 89% |
E9AMS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 89% |