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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HBI6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.622 |
CLV_PCSK_FUR_1 | 367 | 371 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.666 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.602 |
DEG_APCC_DBOX_1 | 386 | 394 | PF00400 | 0.475 |
DOC_CKS1_1 | 358 | 363 | PF01111 | 0.597 |
DOC_CKS1_1 | 8 | 13 | PF01111 | 0.644 |
DOC_CYCLIN_RxL_1 | 110 | 117 | PF00134 | 0.616 |
DOC_CYCLIN_yClb3_PxF_3 | 198 | 204 | PF00134 | 0.615 |
DOC_CYCLIN_yCln2_LP_2 | 386 | 392 | PF00134 | 0.312 |
DOC_MAPK_gen_1 | 367 | 376 | PF00069 | 0.686 |
DOC_MAPK_gen_1 | 403 | 410 | PF00069 | 0.364 |
DOC_MAPK_gen_1 | 59 | 66 | PF00069 | 0.610 |
DOC_PP1_RVXF_1 | 371 | 377 | PF00149 | 0.409 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.734 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.676 |
DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.644 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.621 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 187 | 192 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.683 |
LIG_Actin_WH2_2 | 173 | 189 | PF00022 | 0.620 |
LIG_BIR_III_2 | 75 | 79 | PF00653 | 0.622 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.735 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.659 |
LIG_CtBP_PxDLS_1 | 31 | 37 | PF00389 | 0.609 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.615 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.683 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.724 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.570 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.641 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.754 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.620 |
LIG_LIR_Apic_2 | 258 | 264 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 201 | 208 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.678 |
LIG_NRBOX | 380 | 386 | PF00104 | 0.279 |
LIG_NRBOX | 403 | 409 | PF00104 | 0.414 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.728 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.613 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.610 |
MOD_CDC14_SPxK_1 | 97 | 100 | PF00782 | 0.620 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.601 |
MOD_CDK_SPK_2 | 54 | 59 | PF00069 | 0.604 |
MOD_CDK_SPK_2 | 74 | 79 | PF00069 | 0.778 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 94 | 100 | PF00069 | 0.622 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.617 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.716 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.605 |
MOD_CDK_SPxxK_3 | 7 | 14 | PF00069 | 0.664 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.627 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.735 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.683 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.607 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.640 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.591 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.629 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.791 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.719 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.777 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.661 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.419 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.480 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.569 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.558 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.458 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.492 |
MOD_GlcNHglycan | 217 | 221 | PF01048 | 0.478 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.453 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.385 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.504 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.454 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.451 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.357 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.540 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.591 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.480 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.656 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.715 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.704 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.731 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.641 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.764 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.625 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.771 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.726 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.660 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.710 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.654 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.697 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.710 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.700 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.522 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.421 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.390 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.477 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.465 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.691 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.711 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.385 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.634 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.619 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.709 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.675 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.672 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.601 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.725 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.813 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.548 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.601 |
MOD_PKB_1 | 367 | 375 | PF00069 | 0.623 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.688 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.617 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.662 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.660 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.672 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.624 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.749 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.598 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.673 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.670 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.745 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.600 |
MOD_SUMO_rev_2 | 254 | 262 | PF00179 | 0.673 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.621 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.657 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.629 |
TRG_NES_CRM1_1 | 24 | 38 | PF08389 | 0.679 |
TRG_NES_CRM1_1 | 380 | 394 | PF08389 | 0.231 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8U0 | Leptomonas seymouri | 26% | 95% |
A0A3Q8IHI2 | Leishmania donovani | 56% | 100% |
A4I9Y1 | Leishmania infantum | 55% | 100% |
E9B4Y9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q4Q2Z7 | Leishmania major | 55% | 100% |