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: A4HDL9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.850 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.851 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.799 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.851 |
CLV_PCSK_PC7_1 | 373 | 379 | PF00082 | 0.850 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.779 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.744 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.575 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.569 |
DEG_APCC_DBOX_1 | 547 | 555 | PF00400 | 0.512 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.612 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.465 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.673 |
DOC_CYCLIN_RxL_1 | 140 | 151 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.502 |
DOC_MAPK_NFAT4_5 | 143 | 151 | PF00069 | 0.564 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.825 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.601 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 254 | 264 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 527 | 531 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 546 | 552 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 8 | 26 | PF00022 | 0.667 |
LIG_deltaCOP1_diTrp_1 | 205 | 210 | PF00928 | 0.578 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.664 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.304 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.792 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.555 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.578 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.596 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.704 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.570 |
LIG_GBD_Chelix_1 | 50 | 58 | PF00786 | 0.619 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.614 |
LIG_LYPXL_yS_3 | 19 | 22 | PF13949 | 0.703 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.618 |
LIG_NRBOX | 353 | 359 | PF00104 | 0.564 |
LIG_PCNA_yPIPBox_3 | 70 | 80 | PF02747 | 0.365 |
LIG_Pex14_1 | 531 | 535 | PF04695 | 0.460 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.695 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.489 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.593 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.611 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.594 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.755 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.592 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.573 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.446 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.573 |
LIG_TRAF2_1 | 444 | 447 | PF00917 | 0.571 |
MOD_CDC14_SPxK_1 | 298 | 301 | PF00782 | 0.584 |
MOD_CDK_SPxK_1 | 295 | 301 | PF00069 | 0.585 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.671 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.634 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.585 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.810 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.568 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.850 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.767 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.650 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.552 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.499 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.841 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.703 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.830 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.703 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.571 |
MOD_CMANNOS | 531 | 534 | PF00535 | 0.709 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.513 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.422 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.573 |
MOD_GlcNHglycan | 247 | 252 | PF01048 | 0.605 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.719 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.676 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.618 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.709 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.697 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.515 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.594 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.491 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.679 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.819 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.823 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.669 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.635 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.794 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.747 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.567 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.671 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.608 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.596 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.583 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.576 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.824 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.791 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.554 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.617 |
MOD_N-GLC_2 | 417 | 419 | PF02516 | 0.621 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.339 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.528 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.567 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.609 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.656 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.448 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.578 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.691 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.725 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.666 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.469 |
MOD_PK_1 | 63 | 69 | PF00069 | 0.592 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.497 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.596 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.412 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.508 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.749 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.595 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.561 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.473 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.596 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.584 |
MOD_PKB_1 | 379 | 387 | PF00069 | 0.847 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.822 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.565 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.482 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.403 |
MOD_Plk_2-3 | 483 | 489 | PF00069 | 0.549 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.505 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.513 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.615 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.533 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.525 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.617 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.814 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.473 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.727 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.786 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.672 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.687 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.850 |
TRG_ER_diArg_1 | 546 | 549 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.371 |
TRG_NLS_MonoCore_2 | 375 | 380 | PF00514 | 0.848 |
TRG_NLS_MonoExtC_3 | 375 | 380 | PF00514 | 0.848 |
TRG_NLS_MonoExtN_4 | 373 | 380 | PF00514 | 0.848 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WYG0 | Leishmania donovani | 69% | 100% |
E9AH66 | Leishmania infantum | 69% | 100% |
E9AX04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QAH2 | Leishmania major | 66% | 100% |